{"Abbreviation":["MEAI","5-MeO-AI"],"Aliases":["2-Amino-5-methoxyindan","2-amino-5-methoxyindan","Chaperon","5-Meo-ai","5-methoxyindan-2-ylamine","1H-Inden-2-amine, 2,3-dihydro-5-methoxy-","5-Methoxy-2,3-dihydro-1h-inden-2-amine","MEAI","5-Methoxyindan-2-amine","Mfcd08234971","5-methoxy-2-aminoindan","2-Amino-5-methoxyindane","Schembl295336","Akos006284250","AB43715","SY290731","DB-058122","NS00017992","1H-Inden-2-amine,2,3-dihydro-5-methoxy-,(2S)-(9CI)"],"CAS":"73305-09-6","ChemicalClasses":["2-aminoindane"],"Chirality":"racemic","DTXSID":"80478566","DurationOfAction":"","EliminationHalfLife":"","Erowid Experience Reports":[],"Esters":[],"Formating":[],"HMDB ID":"HMDB0247336","HeavyAtomCount":12,"IUPACName":"5-methoxy-2,3-dihydro-1H-inden-2-amine","InChI":"InChI=1S/C10H13NO/c1-12-10-3-2-7-4-9(11)5-8(7)6-10/h2-3,6,9H,4-5,11H2,1H3","InChIKey":"HLXHCNWEVQNNKA-UHFFFAOYSA-N","MeSH Headers":[],"MolecularFormula":"C\u003csub\u003e10\u003c/sub\u003eH\u003csub\u003e13\u003c/sub\u003eNO","MolecularWeight":"163.22 g/mol","Opticalactivity":"( + / - )","PubChemId":12147687,"PubChemTitle":"2-Amino-5-methoxyindan","Reagents":[],"Record Description":["Wikipedia|List of designer drugs|Empathogens|Miscellaneous polycyclic phenethylamines (Indane and tetralin-type phenethylamines)"],"Records":{"UNII":{"Impurities":[]}},"Reddit Experience Reports":[{"author":"DMTrott","body":"Practise harm reduction. Stay safe.\n\n.\n\n**WHAT IS THE DRUG USERS BIBLE?**\n\nIn a nutshell, it’s a 638 page harm reduction reference tome. From Amazon:\n\n“*Over a 12 year period the author of this book self-administered over 180 psychoactive substances; both chemicals and plants. For each he recorded the life-sensitive safety data, including the anticipated onset times, the common threshold doses, the routes of administration, and the expected duration of the experience. In addition, for every compound he also produced a trip report, detailing the qualitative experience itself. This delivered another invaluable insight, enabling, for example, an objective assessment of the extent of any loss of judgement and self-control.*”\n\n**WHY IS IT NOW A FREE PDF?**\n\nIt was written to reach as many consumers as possible, and ideally, to imbed a harm reduction check-point into the individual’s drug-usage process, whatever their drug of choice. But how to reach the consumer who is perhaps in a social setting and is short on time?\n\nThe answer for many will be via their mobile phones; and the provision of instant access to something the individual actually owns (the PDF). This sense of ownership is undoubtedly a factor in terms of motivation to reference.\n\nFurther, upon opening the PDF there is no requirement to search or to think or to work anything out. All that is needed is a swipe down to that drug of choice.\n\nNote also that the book’s layout was specifically designed with this in mind: for each drug the essential data is at the top of the page, followed by a break in the form of a photograph, and then the ‘delve deeper’ in the form of text and detail.\n\nFor many, this is surely the most cogent scenario in terms of preventing tragedy. It’s possibly as simple as it gets. Alternatively, of course, the PDF can be used on a PC or laptop or wherever is required.\n\n**THE DOWNLOAD LINKS ARE HERE**\n\nYou can currently download it directly from Google Drive, Microsoft Drive, Mega, Apple iCloud and Dropbox. The links are on the following page:\n\n[https://www.drugusersbible.com/2018/01/pdf.html](https://www.drugusersbible.com/2018/01/pdf.html)\n\n**HOW YOU CAN HELP OTHERS**\n\nIt really is vital that we make harm reduction information ubiquitous within our community. It really is ignorance that kills so many of us. We really really must do our best as a community to make safety practices second nature, and get the essential data to everyone who needs it. You can help with this project. Please do help.\n\nIf you are able, please download it and re-upload it to wherever is appropriate: to anywhere from which anyone who uses drugs may see it, and be able to download it themselves for free. Or alternatively just share the download link.\n\nIgnorance kills, but I hope that some of you will help to save some of those lives. The portability of a PDF may help to at least put the idea of harm reduction on the agenda where it was previously overlooked.\n\n**FINALLY**\n\nTogether, let’s try to make a difference. If you have any questions, at all, please don’t hesitate to ask.\n\n.\n\n# THIS IS THE TABLE OF CONTENTS FROM THE BOOK ITSELF:\n\n**1. DRUGSCAPE: AN INTRODUCTION**\n\n1.1 Safety First\n\n1.1.1 The 10 Commandments\n\n1.1.2 How To Use A Drug Testing Kit\n\n1.2 Interpreting the Reports\n\n1.2.1 Definition of Terms\n\n1.2.2 The Shulgin Rating Scale\n\n1.2.3 Classification\n\n1.2.4 Routes of Administration (RoA)\n\n1.2.5 More On Source \u0026 Jurisdiction\n\n1.3 General Safety Notes\n\n1.3.1 If You Are Not An Adult\n\n1.3.2 Risk Mitigation For IV\n\n1.3.3 Nasal Care\n\n1.3.4 Chemsex\n\n1.3.5 What Goes Up Must Come Down\n\n1.3.6 Complacency Kills\n\n**2. CHEMSCAPE: A CHEMICAL JOURNEY**\n\n2.1 Introduction\n\n2.2 Psychedelics\n\n2.2.1 1P-LSD\n\n2.2.2 1cP-LSD\n\n2.2.3 1P-ETH-LAD\n\n2.2.4 2C-B\n\n2.2.5 2C-B-AN\n\n2.2.6 2C-B-FLY\n\n2.2.7 2C-E\n\n2.2.8 2C-I\n\n2.2.9 4-ACO-DMT\n\n2.2.10 4-HO-MET\n\n2.2.11 5-MeO-DALT\n\n2.2.12 5-MeO-DIBF\n\n2.2.13 AL-LAD\n\n2.2.14 AMT\n\n2.2.15 BK-2C-B\n\n2.2.16 Changa\n\n2.2.17 DMT\n\n2.2.18 DOM\n\n2.2.19 LSD\n\n2.2.20 LSZ\n\n2.2.21 TMA\n\n2.3 Stimulants\n\n2.3.1 2AI\n\n2.3.2 3,4 CTMP\n\n2.3.3 3-FPM\n\n2.3.4 3-MMC\n\n2.3.5 4-FA\n\n2.3.6 4-Me-TMP\n\n2.3.7 4F-EPH\n\n2.3.8 4F-MPH\n\n2.3.9 Adderall\n\n2.3.10 Amphetamine\n\n2.3.11 a-PHP\n\n2.3.12 Caffeine\n\n2.3.13 Cocaine\n\n2.3.14 EPH\n\n2.3.15 HDMP-28\n\n2.3.16 Hexen\n\n2.3.17 IPPH\n\n2.3.18 Methamphetamine\n\n2.3.19 Methylphenidate\n\n2.3.20 MPA\n\n2.3.21 NM2AI\n\n2.3.22 PPH\n\n2.3.23 Pipradrol\n\n2.3.24 TPA\n\n2.4 Anxiolytics \u0026 Sedatives\n\n2.4.1 Alprazolam\n\n2.4.2 Carisoprodol\n\n2.4.3 Clonazolam\n\n2.4.4 Diazepam\n\n2.4.5 Etizolam\n\n2.4.6 Gabapentin\n\n2.4.7 Pregabalin\n\n2.4.8 Pyrazolam\n\n2.4.9 Zopiclone\n\n2.4.10 Others\n\n2.5 Intoxicating Depressants\n\n2.5.1 Alcohol\n\n2.5.2 Codeine\n\n2.5.3 Fentanyl\n\n2.5.4 GHB\n\n2.5.5 Heroin\n\n2.5.6 Lean\n\n2.5.7 Morphine\n\n2.5.8 Oxycodone\n\n2.5.9 Poppers\n\n2.5.10 Sentia\n\n2.5.11 Tramadol\n\n2.6 Dissociatives\n\n2.6.1 3-Ho-PCP\n\n2.6.2 3-MeO-PCMo\n\n2.6.3 Diphenidine\n\n2.6.4 DXM\n\n2.6.5 Ephenidine\n\n2.6.6 Ketamine\n\n2.6.7 Mefloquine\n\n2.6.8 MXE\n\n2.6.9 MXP\n\n2.6.10 N2O\n\n2.7 Empathogens \u0026 Entactogens\n\n2.7.1 6-APB\n\n2.7.2 MDA\n\n2.7.3 MDAI\n\n2.7.4 MDMA\n\n2.7.5 MEAI\n\n2.7.6 Mephedrone\n\n2.7.7 Methylone\n\n2.7.8 MNA\n\n2.7.9 Mexedrone\n\n2.8 Synthetic Cannabinoids\n\n2.8.1 5F-AKB48\n\n2.8.2 AM-2201\n\n2.8.3 AM-694\n\n2.8.4 JWH-018\n\n2.8.5 JWH-073\n\n2.9 Nootropics\n\n2.9.1 5-HTP\n\n2.9.2 Aniracetam + Citicoline\n\n2.9.3 Armodafinil\n\n2.9.4 L-Theanine\n\n2.9.5 Modafiendz\n\n2.9.6 Modafinil\n\n2.9.7 Noopept\n\n2.9.8 NSI 189\n\n2.9.9 Phenibut\n\n2.9.10 Picamilon\n\n2.9.11 PRL-8-53\n\n**3. BOTSCAPE: A BOTANICAL JOURNEY**\n\n3.1 Introduction\n\n3.2 Psychedelics\n\n3.2.1 Ayahuasca\n\n3.2.2 Cebil\n\n3.2.3 Chaliponga Leaves\n\n3.2.4 Fly Agaric\n\n3.2.5 HBWS\n\n3.2.6 Iboga\n\n3.2.7 Magic Mushrooms\n\n3.2.8 Magic Truffles\n\n3.2.9 Morning Glory Seeds\n\n3.2.10 Ololiuqui\n\n3.2.11 Salvia\n\n3.2.12 Sananga\n\n3.2.13 San Pedro Cactus\n\n3.2.14 Sensory Deprivation\n\n3.2.15 Shirodhara\n\n3.2.16 Sinicuichi\n\n3.2.17 Syrian Rue\n\n3.2.18 Yopo\n\n3.3 Stimulants\n\n3.3.1 Betel Nut\n\n3.3.2 Coca\n\n3.3.3 Ephedra\n\n3.3.4 Ginseng\n\n3.3.5 Green Tea\n\n3.3.6 Guarana\n\n3.3.7 Guayusa\n\n3.3.8 Horny Goat Weed\n\n3.3.9 Khaini\n\n3.3.10 Kola Nut\n\n3.3.11 Wormwood\n\n3.3.12 Yerba Mate\n\n3.3.13 Yohimbe\n\n3.4 Sedatives\n\n3.4.1 Blue Lotus\n\n\\[Pink Lotus Flower, Red Lily\\]\n\n3.4.2 Cacao\n\n3.4.3 Catnip\n\n3.4.4 Chamomile\n\n3.4.5 Damiana\n\n3.4.6 Frankincense\n\n3.4.7 Hops\n\n3.4.8 Imphepho\n\n3.4.9 Indian Warrior\n\n3.4.10 Kanna\n\n3.4.11 Lavender\n\n3.4.12 Maconha Brava\n\n3.4.13 Marihuanilla\n\n3.4.14 Mullein\n\n3.4.15 Mulungu\n\n3.4.16 Passion Flower\n\n3.4.17 Rhodiola\n\n3.4.18 Saffron\n\n3.4.19 St. John's Wort\n\n3.4.20 Skullcap\n\n3.4.21 Valerian Root\n\n3.4.22 White Sage\n\n3.4.23 Wild Dagga\n\n3.4.24 Wild Lettuce\n\n3.5 Nootropics\n\n3.5.1 Catuaba\n\n3.5.2 Celastrus Paniculatus\n\n3.5.3 Ginkgo\n\n3.6 Oneirogens\n\n3.6.1 Calea\n\n3.6.2 Entada Rheedii\n\n3.6.3 Mexican Tarragon\n\n3.6.4 Mugwort\n\n3.6.5 Ubulawu\n\n3.7 Deliriants\n\n3.7.1 Datura\n\n3.7.2 Nutmeg\n\n3.8 Unclassified\n\n3.8.1 Cannabis\n\n3.8.2 Essential Oils\n\n3.8.3 Kava Kava\n\n3.8.4 Kratom\n\n3.8.5 Mad Honey\n\n3.8.6 Mapacho\n\n3.8.7 Opium\n\n3.8.8 Rapé\n\n3.8.9 Sakae Naa\n\n3.8.10 Tobacco\n\n**4. WORLDSCAPE: THE WIDER CONTEXT**\n\n4.1 How Many People Use Drugs?\n\n4.2 The Relative Harm\n\n4.3 Addiction \u0026 Overdose\n\n4.3.1 Addiction\n\n4.3.2 If You Are Addicted\n\n4.3.3 Alcoholism\n\n4.3.4 Overdose \u0026 Emergency Response\n\n4.3.5 Drug Related Deaths: Notable People\n\n4.4 The LawScape\n\n4.4.1 The United Kingdom\n\n4.4.2 The United States\n\n4.4.3 The Rest of The World\n\n4.4.4 Dealers: A Different Perspective\n\n4.4.5 The Role of The Media\n\n4.4.6 Mandatory Drug Testing\n\n4.4.7 Activism: The Charter of Drug Users Rights\n\n4.5 Drug Tourism\n\n4.5.1 The Dutch Connection\n\n4.5.2 Global Snapshots\n\n4.6 Culture \u0026 Society (Reference)\n\n4.6.1 Art, Film, Literature, Music\n\n4.6.2 Food For The Psychedelic Mind\n\n4.6.3 Books \u0026 Reference\n\n4.7 Confessions of a Lab Rat\n\n4.7.1 Q\u0026A\n\n4.7.2 About The Author – In His Own Words\n\n4.8 Argot\n\n4.8.1 Idioms \u0026 Acronyms\n\n4.8.2 Common, Street \u0026 Brand Names\n\n4.8.3 Poly Drug Combinations\n\n4.8.4 Selected Molecules\n\n4.8.5 Alphabetical Index\n\n4.9 Internet Resources\n\n4.9.1 Harm Reduction \u0026 Safety\n\n4.9.2 The Drug Users Bible\n\n4.10 Supplementary Notes\n\n4.11 Supplementary Photographs\n\n4.12 Namaste: A Final Note\n\nEpilogue \u0026 The Last Word","body_length":8078,"dose_notes":["no dose information found"],"doselog":null,"doses":null,"flair":"Other","headers":null,"id":"15b26m0","num_comments":1,"prep_flags":null,"pubdate":"2023-07-27","routes":["intravenous"],"score":3,"substances":["1P-ETH-LAD","1P-LSD","1cP-LSD","2C-B","2C-B-Fly","2C-E","2C-I","3-HO-PCP","3-MeO-PCMo","4-AcO-DMT","4-HO-MET","5-MeO-DALT","5-MeO-DiBF","5F-AKB48","6-APB","AL-LAD","AM-2201","AMT","Alcohol","Alprazolam","Amphetamine","Aniracetam","Armodafinil","Ayahuasca","Betel Nut","Caffeine","Cannabinoids","Cannabis","Carisoprodol","Catnip","Catuaba","Chamomile","Changa","Citicoline","Clonazolam","Cocaine","Codeine","DALT","DMT","DXM","Damiana","Datura","Diazepam","Diphenidine","ETH-LAD","Entada rheedii","Ephenidine","Etizolam","Fentanyl","Frankincense","GHB","Gabapentin","Ginseng","Guarana","HDMP-28","Heroin","Ibogaine","Indian Warrior","JWH-018","JWH-073","Kanna","Ketamine","Kola Nut","Kratom","LSD","LSZ","MDA","MDAI","MDMA","MEAI","Mefloquine","Methamphetamine","Methoxetamine","Methylone","Methylphenidate","Mexedrone","Modafinil","Morning Glory","Morphine","Mugwort","Mullein","Noopept","Nutmeg","Oxycodone","PCP","PRL-8-53","Passion Flower","Picamilon","Pregabalin","Psilocybin Mushrooms","Pyrazolam","Sakae Naa","Salvia divinorum","Skullcap","St. John's Wort","Syrian Rue","TMA","Theanine","Tobacco","Tramadol","Valerian","Wormwood","Yerba Mate","Yohimbe","Zopiclone","bk-2C-B"],"time_format":null,"title":"There are 45 psychedelic and dissociative trip reports in the Drug Users Bible: Download a free copy from here. Whether psychedelics are used for recreation, you need to look after yourself. Stay safe.","upvote_ratio":1,"url":"https://reddit.com/r/tripreports/comments/15b26m0/there_are_45_psychedelic_and_dissociative_trip/"}],"RefChem":"85279","RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/MEAI","Name":"5-Methoxy-2-aminoindane","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q21098822","Name":"5-Methoxy-2-aminoindane","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/12147687","Name":"5-Methoxy-2-aminoindane","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=73305-09-6","Name":"5-Methoxy-2-aminoindane","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0247336","Name":"5-Methoxy-2-aminoindane","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/AD8S15863A","Name":"5-Methoxy-2-aminoindane","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID80478566","Name":"5-Methoxy-2-aminoindane","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 12147687, 5-Methoxy-2-aminoindane. Accessed June 3, 2026. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/12147687\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/12147687\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 5-Methoxy-2-aminoindane. UNII: AD8S15863A. Global Substance Registration System. Accessed June 3, 2026. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/AD8S15863A\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/AD8S15863A\u003c/a\u003e"],"SMILES":"COC1=CC2=C(CC(C2)N)C=C1","SaltData":[],"Salts":[],"Scheduling":[{"act":"Neue-psychoaktive-Stoffe-Gesetz (NpSG)","gov":"Germany","ref":[],"schedule":"Neuer-Psychoaktiver-Stoff"},{"gov":"United Kingdom","ref":[],"schedule":"PSA substance"}],"StereoisomerData":[{"ChemicalClasses":["2-aminoindane"],"SMILES":"COC1=CC2=C(C=C1)C[C@@H](N)C2","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 101.942 34.741\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg fill=\"#3050f8\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".8\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h102v35H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m1.106 10.77 9.588-5.533M17.914 5.236l9.589 5.539\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m40.711 3.155-13.208 7.62M40.711 5.97l-10.77 6.213\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.711 3.155 13.208 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M53.919 26.015v-15.24M51.481 24.606V12.183\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.919 26.015-13.208 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.503 26.015 13.208 7.62M29.941 24.606l10.77 6.214\"/\u003e\u003c/g\u003e\u003cpath d=\"M27.503 10.775v15.24M53.919 26.015l14.529 4.673M68.448 30.688l8.941-12.293\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M77.389 17.995v.8M79.929 17.661v1.467M82.469 17.328v2.134M85.009 16.995v2.8M87.549 16.661v3.467\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"M85.009 16.995v1.4M87.549 16.661v1.734M87.549 16.661v1.734\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"M77.389 18.395 68.448 6.101M53.919 10.775l14.529-4.674\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M14.309 1.108q-.738 0-1.173.553-.429.548-.429 1.495 0 .946.429 1.494.435.547 1.173.547t1.167-.547q.428-.548.428-1.494 0-.947-.428-1.495-.429-.553-1.167-.553m0-.548q1.054 0 1.679.708.631.703.631 1.888 0 1.178-.631 1.887-.625.702-1.679.702t-1.685-.702q-.631-.703-.631-1.887t.631-1.888Q13.255.56 14.309.56\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M90.735 15.894h.911l2.215 4.185v-4.185h.661v5.001h-.911L91.39 16.71v4.185h-.655zM95.093 15.894h.679v2.048h2.458v-2.048h.673v5.001h-.673v-2.381h-2.458v2.381h-.679zM99.964 22.079h1.418v.343h-1.907v-.343q.232-.239.628-.639.4-.404.504-.522.196-.218.271-.368.079-.153.079-.3 0-.239-.168-.389t-.436-.15q-.193 0-.403.068-.211.064-.454.196v-.407q.246-.1.457-.15.215-.05.39-.05.467 0 .743.232.278.232.278.625 0 .182-.071.35-.068.165-.25.39-.05.057-.322.335-.268.279-.757.779\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M10.694 5.237 5.9 8.003M17.914 5.236l4.795 2.769\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(R)-5-Methoxy-2-aminoindane"},{"ChemicalClasses":["2-aminoindane"],"SMILES":"COC1=CC2=C(C=C1)C[C@H](N)C2","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 101.942 34.741\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg fill=\"#3050f8\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".8\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h102v35H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m1.106 10.77 9.588-5.533M17.914 5.236l9.589 5.539\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m40.711 3.155-13.208 7.62M40.711 5.97l-10.77 6.213\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.711 3.155 13.208 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M53.919 26.015v-15.24M51.481 24.606V12.183\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.919 26.015-13.208 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.503 26.015 13.208 7.62M29.941 24.606l10.77 6.214\"/\u003e\u003c/g\u003e\u003cpath d=\"M27.503 10.775v15.24M53.919 26.015l14.529 4.673M68.448 30.688l8.941-12.293\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"M77.389 17.995v.8l11.746 1.542v-3.884z\" class=\"bond\"/\u003e\u003cpath d=\"M77.389 18.395 68.448 6.101M53.919 10.775l14.529-4.674\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M14.309 1.108q-.738 0-1.173.553-.429.548-.429 1.495 0 .946.429 1.494.435.547 1.173.547t1.167-.547q.428-.548.428-1.494 0-.947-.428-1.495-.429-.553-1.167-.553m0-.548q1.054 0 1.679.708.631.703.631 1.888 0 1.178-.631 1.887-.625.702-1.679.702t-1.685-.702q-.631-.703-.631-1.887t.631-1.888Q13.255.56 14.309.56\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M90.735 15.894h.911l2.215 4.185v-4.185h.661v5.001h-.911L91.39 16.71v4.185h-.655zM95.093 15.894h.679v2.048h2.458v-2.048h.673v5.001h-.673v-2.381h-2.458v2.381h-.679zM99.964 22.079h1.418v.343h-1.907v-.343q.232-.239.628-.639.4-.404.504-.522.196-.218.271-.368.079-.153.079-.3 0-.239-.168-.389t-.436-.15q-.193 0-.403.068-.211.064-.454.196v-.407q.246-.1.457-.15.215-.05.39-.05.467 0 .743.232.278.232.278.625 0 .182-.071.35-.068.165-.25.39-.05.057-.322.335-.268.279-.757.779\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M10.694 5.237 5.9 8.003M17.914 5.236l4.795 2.769\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(S)-5-Methoxy-2-aminoindane"}],"StereoisomerType":"enantiomer","Stereoisomers":["(R)-5-Methoxy-2-aminoindane","(S)-5-Methoxy-2-aminoindane"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 101.942 34.741\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg fill=\"#3050f8\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".8\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h102v35H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m1.106 10.77 9.588-5.533M17.914 5.236l9.589 5.539\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m40.711 3.155-13.208 7.62M40.711 5.97l-10.77 6.213\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.711 3.155 13.208 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M53.919 26.015v-15.24M51.481 24.606V12.183\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.919 26.015 14.529 4.673M68.448 30.688l8.941-12.293M77.389 18.395 68.448 6.101M53.919 10.775l14.529-4.674M77.389 18.395h11.746M53.919 26.015l-13.208 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m27.503 26.015 13.208 7.62M29.941 24.606l10.77 6.214\"/\u003e\u003c/g\u003e\u003cpath d=\"M27.503 10.775v15.24\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M14.309 1.108q-.738 0-1.173.553-.429.548-.429 1.495 0 .946.429 1.494.435.547 1.173.547t1.167-.547q.428-.548.428-1.494 0-.947-.428-1.495-.429-.553-1.167-.553m0-.548q1.054 0 1.679.708.631.703.631 1.888 0 1.178-.631 1.887-.625.702-1.679.702t-1.685-.702q-.631-.703-.631-1.887t.631-1.888Q13.255.56 14.309.56\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M90.735 15.894h.911l2.215 4.185v-4.185h.661v5.001h-.911L91.39 16.71v4.185h-.655zM95.093 15.894h.679v2.048h2.458v-2.048h.673v5.001h-.673v-2.381h-2.458v2.381h-.679zM99.964 22.079h1.418v.343h-1.907v-.343q.232-.239.628-.639.4-.404.504-.522.196-.218.271-.368.079-.153.079-.3 0-.239-.168-.389t-.436-.15q-.193 0-.403.068-.211.064-.454.196v-.407q.246-.1.457-.15.215-.05.39-.05.467 0 .743.232.278.232.278.625 0 .182-.071.35-.068.165-.25.39-.05.057-.322.335-.268.279-.757.779\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M10.694 5.237 5.9 8.003M17.914 5.236l4.795 2.769\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"M89.135 18.395h-5.873M89.135 18.395h-5.873\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"5-Methoxy-2-aminoindane","UNII":"AD8S15863A","Wikidata":"Q21098822","Wikipedia":"MEAI","XLogP":1.3}
