{"Abbreviation":["3-CPM"],"Aliases":["3-Cpm","PAL-594","Morpholine, 2-(3-chlorophenyl)-3-methyl-","CS-0283434","En300-303778"],"CAS":"1097796-78-5","ChemicalClasses":["phenylmorpholine"],"Chirality":"racemic","DBI-IGS":"3-CPM","Dosing Info":[],"Esters":[],"Formating":[],"HeavyAtomCount":14,"IUPACName":"2-(3-chlorophenyl)-3-methylmorpholine","InChI":"InChI=1S/C11H14ClNO/c1-8-11(14-6-5-13-8)9-3-2-4-10(12)7-9/h2-4,7-8,11,13H,5-6H2,1H3","InChIKey":"BOFUZZAQNVYZFF-UHFFFAOYSA-N","MolecularFormula":"C\u003csub\u003e11\u003c/sub\u003eH\u003csub\u003e14\u003c/sub\u003eClNO","MolecularWeight":"211.69 g/mol","Opticalactivity":"UNSPECIFIED","PD":"PD150693","PubChemId":43350791,"Record Description":["Wikipedia|List of designer drugs|Stimulants|Phenylmorpholines"],"RefChem":"93525","RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/3-Chlorophenmetrazine","Name":"3-Chlorophenmetrazine","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q108530213","Name":"3-Chlorophenmetrazine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/43350791","Name":"3-Chlorophenmetrazine","Sub":false}]},{"Name":"Probes \u0026 Drugs","Urls":[{"Link":"https://www.probes-drugs.org/compound/PD150693","Name":"3-Chlorophenmetrazine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=1097796-78-5","Name":"3-Chlorophenmetrazine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/B6P88Q2VW5","Name":"3-Chlorophenmetrazine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID701337061","Name":"3-Chlorophenmetrazine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 43350791, 3-Chlorophenmetrazine. Accessed October 14, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/43350791\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/43350791\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 3-Chlorophenmetrazine. UNII: B6P88Q2VW5. Global Substance Registration System. Accessed October 14, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/B6P88Q2VW5\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/B6P88Q2VW5\u003c/a\u003e"],"SMILES":"CC1C(OCCN1)C2=CC(=CC=C2)Cl","SaltData":[],"Salts":[],"StereoisomerData":[{"Aliases":null,"PubChemId":null,"SMILES":"C[C@H]1NCCO[C@@H]1C1=CC(Cl)=CC=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 85.573 62.826\"\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=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h86v63H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"m57.959 16.388.35-.607-12.313-9.135-1.051 1.818-1.05 1.819z\" class=\"bond\"/\u003e\u003cpath d=\"m58.134 16.084 10.048-5.794M74.489 10.291l10.046 5.798M84.535 16.089l-.002 15.231M84.533 31.32l-9.923 5.723M68.047 37.038l-9.916-5.722M58.134 16.084l-.003 15.232\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m58.306 31.619-.35-.606M56.254 33.141l-.642-1.111M54.201 34.663l-.933-1.617M52.148 36.185l-1.225-2.122M50.096 37.707l-1.517-2.627M48.043 39.229l-1.808-3.133M45.99 40.751l-2.1-3.638\"/\u003e\u003c/g\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m44.94 38.932-13.195-7.624M42.502 40.339l-10.758-6.216\"/\u003e\u003c/g\u003e\u003cpath d=\"m31.745 31.308-13.191 7.615M18.554 38.923l-11.679-6.74\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m18.554 38.923.005 15.24M20.993 40.331l.004 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m18.559 54.163 13.195 7.625\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m31.754 61.788 13.191-7.616M31.755 58.972l10.751-6.208\"/\u003e\u003c/g\u003e\u003cpath d=\"m44.94 38.932.005 15.24\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M73.276 10.921h-.72l-2.619-4.066h-.03l.03.595q.023.357.023.732v2.739h-.565v-4.9h.714l2.608 4.054h.029l-.017-.327-.024-.476q-.006-.262-.006-.483V6.021h.577zM73.139 5.459h-.619V3.173h-2.512v2.286h-.613V.56h.613v2.072h2.512V.56h.619z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M73.59 38.931q0 .756-.256 1.327-.256.566-.756.882-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.887-.245-.572-.245-1.334 0-.75.245-1.31.25-.565.756-.881.506-.315 1.274-.315.732 0 1.232.315.5.31.756.875.256.566.256 1.328m-3.864 0q0 .923.387 1.458.393.53 1.221.53.839 0 1.22-.53.387-.535.387-1.458 0-.929-.387-1.453-.381-.524-1.208-.524-.834 0-1.227.524t-.393 1.453\" class=\"atom\"/\u003e\u003cpath fill=\"#1ff01f\" stroke=\"none\" d=\"M2.906 29.494q-.786 0-1.239.53-.452.524-.452 1.446 0 .911.417 1.447.422.53 1.268.53.321 0 .607-.054.291-.059.565-.143v.536q-.274.101-.565.149-.292.054-.697.054-.744 0-1.25-.31-.5-.31-.75-.875-.25-.572-.25-1.34 0-.744.268-1.309.274-.566.804-.881.529-.322 1.279-.322.78 0 1.352.286l-.244.524q-.226-.101-.506-.185-.274-.083-.607-.083m2.756 4.423h-.601v-5.215h.601z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m68.182 10.29-5.024 2.897M68.182 10.29l-5.024 2.897M74.489 10.291l5.023 2.899M74.489 10.291l5.023 2.899\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m74.61 37.043 4.962-2.862M68.047 37.038l-4.958-2.861\" class=\"hi\"/\u003e\u003cpath stroke=\"#1ff01f\" d=\"m6.875 32.183 5.839 3.37\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(1R,2R)-3-Chlorophenmetrazine","UNII":null},{"Aliases":null,"PubChemId":null,"SMILES":"C[C@@H]1NCCO[C@@H]1C1=CC(Cl)=CC=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 85.573 62.826\"\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=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h86v63H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m57.959 16.388.35-.607M55.615 15.37l.642-1.111M53.271 14.353l.934-1.617M50.927 13.335l1.225-2.121M48.583 12.318 50.1 9.691M46.239 11.3l1.809-3.132M43.895 10.283l2.101-3.637\"/\u003e\u003c/g\u003e\u003cpath d=\"m58.134 16.084 10.048-5.794M74.489 10.291l10.046 5.798M84.535 16.089l-.002 15.231M84.533 31.32l-9.923 5.723M68.047 37.038l-9.916-5.722M58.134 16.084l-.003 15.232\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m58.306 31.619-.35-.606M56.254 33.141l-.642-1.111M54.201 34.663l-.933-1.617M52.148 36.185l-1.225-2.122M50.096 37.707l-1.517-2.627M48.043 39.229l-1.808-3.133M45.99 40.751l-2.1-3.638\"/\u003e\u003c/g\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m44.94 38.932-13.195-7.624M42.502 40.339l-10.758-6.216\"/\u003e\u003c/g\u003e\u003cpath d=\"m31.745 31.308-13.191 7.615M18.554 38.923l-11.679-6.74\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m18.554 38.923.005 15.24M20.993 40.331l.004 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m18.559 54.163 13.195 7.625\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m31.754 61.788 13.191-7.616M31.755 58.972l10.751-6.208\"/\u003e\u003c/g\u003e\u003cpath d=\"m44.94 38.932.005 15.24\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M73.276 10.921h-.72l-2.619-4.066h-.03l.03.595q.023.357.023.732v2.739h-.565v-4.9h.714l2.608 4.054h.029l-.017-.327-.024-.476q-.006-.262-.006-.483V6.021h.577zM73.139 5.459h-.619V3.173h-2.512v2.286h-.613V.56h.613v2.072h2.512V.56h.619z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M73.59 38.931q0 .756-.256 1.327-.256.566-.756.882-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.887-.245-.572-.245-1.334 0-.75.245-1.31.25-.565.756-.881.506-.315 1.274-.315.732 0 1.232.315.5.31.756.875.256.566.256 1.328m-3.864 0q0 .923.387 1.458.393.53 1.221.53.839 0 1.22-.53.387-.535.387-1.458 0-.929-.387-1.453-.381-.524-1.208-.524-.834 0-1.227.524t-.393 1.453\" class=\"atom\"/\u003e\u003cpath fill=\"#1ff01f\" stroke=\"none\" d=\"M2.906 29.494q-.786 0-1.239.53-.452.524-.452 1.446 0 .911.417 1.447.422.53 1.268.53.321 0 .607-.054.291-.059.565-.143v.536q-.274.101-.565.149-.292.054-.697.054-.744 0-1.25-.31-.5-.31-.75-.875-.25-.572-.25-1.34 0-.744.268-1.309.274-.566.804-.881.529-.322 1.279-.322.78 0 1.352.286l-.244.524q-.226-.101-.506-.185-.274-.083-.607-.083m2.756 4.423h-.601v-5.215h.601z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m68.182 10.29-5.024 2.897M68.182 10.29l-5.024 2.897M74.489 10.291l5.023 2.899M74.489 10.291l5.023 2.899\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m74.61 37.043 4.962-2.862M68.047 37.038l-4.958-2.861\" class=\"hi\"/\u003e\u003cpath stroke=\"#1ff01f\" d=\"m6.875 32.183 5.839 3.37\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(1S,2R)-3-Chlorophenmetrazine","UNII":null},{"Aliases":null,"PubChemId":null,"SMILES":"C[C@H]1NCCO[C@H]1C1=CC(Cl)=CC=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 85.573 62.826\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h86v63H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath stroke=\"none\" d=\"m57.959 16.388.35-.607-12.313-9.135-1.051 1.818-1.05 1.819z\" class=\"bond\"/\u003e\u003cpath d=\"m58.134 16.084 10.048-5.794M74.489 10.291l10.046 5.798M84.535 16.089l-.002 15.231M84.533 31.32l-9.923 5.723M68.047 37.038l-9.916-5.722M58.134 16.084l-.003 15.232\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"m58.306 31.619-.35-.606-15.264 6.62 2.248 1.299v2.597z\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m44.94 38.932-13.195-7.624M42.502 40.339l-10.758-6.216\"/\u003e\u003c/g\u003e\u003cpath d=\"m31.745 31.308-13.191 7.615M18.554 38.923l-11.679-6.74\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m18.554 38.923.005 15.24M20.993 40.331l.004 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m18.559 54.163 13.195 7.625\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m31.754 61.788 13.191-7.616M31.755 58.972l10.751-6.208\"/\u003e\u003c/g\u003e\u003cpath d=\"m44.94 38.932.005 15.24\" class=\"bond\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M73.276 10.921h-.72l-2.619-4.066h-.03l.03.595q.023.357.023.732v2.739h-.565v-4.9h.714l2.608 4.054h.029l-.017-.327-.024-.476q-.006-.262-.006-.483V6.021h.577zM73.139 5.459h-.619V3.173h-2.512v2.286h-.613V.56h.613v2.072h2.512V.56h.619z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M73.59 38.931q0 .756-.256 1.327-.256.566-.756.882-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.887-.245-.572-.245-1.334 0-.75.245-1.31.25-.565.756-.881.506-.315 1.274-.315.732 0 1.232.315.5.31.756.875.256.566.256 1.328m-3.864 0q0 .923.387 1.458.393.53 1.221.53.839 0 1.22-.53.387-.535.387-1.458 0-.929-.387-1.453-.381-.524-1.208-.524-.834 0-1.227.524t-.393 1.453\" class=\"atom\"/\u003e\u003cpath fill=\"#1ff01f\" stroke=\"none\" d=\"M2.906 29.494q-.786 0-1.239.53-.452.524-.452 1.446 0 .911.417 1.447.422.53 1.268.53.321 0 .607-.054.291-.059.565-.143v.536q-.274.101-.565.149-.292.054-.697.054-.744 0-1.25-.31-.5-.31-.75-.875-.25-.572-.25-1.34 0-.744.268-1.309.274-.566.804-.881.529-.322 1.279-.322.78 0 1.352.286l-.244.524q-.226-.101-.506-.185-.274-.083-.607-.083m2.756 4.423h-.601v-5.215h.601z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m68.182 10.29-5.024 2.897M68.182 10.29l-5.024 2.897M74.489 10.291l5.023 2.899M74.489 10.291l5.023 2.899\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m74.61 37.043 4.962-2.862M68.047 37.038l-4.958-2.861\" class=\"hi\"/\u003e\u003cpath stroke=\"#1ff01f\" d=\"m6.875 32.183 5.839 3.37\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(1R,2S)-3-Chlorophenmetrazine","UNII":null},{"Aliases":null,"PubChemId":null,"SMILES":"C[C@@H]1NCCO[C@H]1C1=CC(Cl)=CC=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 85.573 62.826\"\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=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h86v63H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m57.959 16.388.35-.607M55.615 15.37l.642-1.111M53.271 14.353l.934-1.617M50.927 13.335l1.225-2.121M48.583 12.318 50.1 9.691M46.239 11.3l1.809-3.132M43.895 10.283l2.101-3.637\"/\u003e\u003c/g\u003e\u003cpath d=\"m58.134 16.084 10.048-5.794M74.489 10.291l10.046 5.798M84.535 16.089l-.002 15.231M84.533 31.32l-9.923 5.723M68.047 37.038l-9.916-5.722M58.134 16.084l-.003 15.232\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"m58.306 31.619-.35-.606-15.264 6.62 2.248 1.299v2.597z\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m44.94 38.932-13.195-7.624M42.502 40.339l-10.758-6.216\"/\u003e\u003c/g\u003e\u003cpath d=\"m31.745 31.308-13.191 7.615M18.554 38.923l-11.679-6.74\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m18.554 38.923.005 15.24M20.993 40.331l.004 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m18.559 54.163 13.195 7.625\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m31.754 61.788 13.191-7.616M31.755 58.972l10.751-6.208\"/\u003e\u003c/g\u003e\u003cpath d=\"m44.94 38.932.005 15.24\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M73.276 10.921h-.72l-2.619-4.066h-.03l.03.595q.023.357.023.732v2.739h-.565v-4.9h.714l2.608 4.054h.029l-.017-.327-.024-.476q-.006-.262-.006-.483V6.021h.577zM73.139 5.459h-.619V3.173h-2.512v2.286h-.613V.56h.613v2.072h2.512V.56h.619z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M73.59 38.931q0 .756-.256 1.327-.256.566-.756.882-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.887-.245-.572-.245-1.334 0-.75.245-1.31.25-.565.756-.881.506-.315 1.274-.315.732 0 1.232.315.5.31.756.875.256.566.256 1.328m-3.864 0q0 .923.387 1.458.393.53 1.221.53.839 0 1.22-.53.387-.535.387-1.458 0-.929-.387-1.453-.381-.524-1.208-.524-.834 0-1.227.524t-.393 1.453\" class=\"atom\"/\u003e\u003cpath fill=\"#1ff01f\" stroke=\"none\" d=\"M2.906 29.494q-.786 0-1.239.53-.452.524-.452 1.446 0 .911.417 1.447.422.53 1.268.53.321 0 .607-.054.291-.059.565-.143v.536q-.274.101-.565.149-.292.054-.697.054-.744 0-1.25-.31-.5-.31-.75-.875-.25-.572-.25-1.34 0-.744.268-1.309.274-.566.804-.881.529-.322 1.279-.322.78 0 1.352.286l-.244.524q-.226-.101-.506-.185-.274-.083-.607-.083m2.756 4.423h-.601v-5.215h.601z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m68.182 10.29-5.024 2.897M68.182 10.29l-5.024 2.897M74.489 10.291l5.023 2.899M74.489 10.291l5.023 2.899\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m74.61 37.043 4.962-2.862M68.047 37.038l-4.958-2.861\" class=\"hi\"/\u003e\u003cpath stroke=\"#1ff01f\" d=\"m6.875 32.183 5.839 3.37\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(1S,2S)-3-Chlorophenmetrazine","UNII":null}],"StereoisomerType":"diastereomer","Stereoisomers":["(1R,2R)-3-Chlorophenmetrazine","(1S,2R)-3-Chlorophenmetrazine","(1R,2S)-3-Chlorophenmetrazine","(1S,2S)-3-Chlorophenmetrazine"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 91.325 55.414\"\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=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h92v56H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m71.328 46.75-.005-15.232M71.323 31.518l-13.192-7.613M58.131 23.905l.002-11.319M61.411 6.77l9.917-5.732M71.328 1.038 84.52 8.652M84.52 8.652l-.001 11.39M71.323 31.518l10.042-5.804M58.131 23.905 44.94 31.52\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m44.94 31.52-13.195-7.624M42.502 32.928l-10.758-6.216\"/\u003e\u003c/g\u003e\u003cpath d=\"m31.745 23.896-13.191 7.616\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m18.554 31.512.005 15.24M20.993 32.919l.004 12.425\"/\u003e\u003c/g\u003e\u003cpath d=\"m18.559 46.752 13.195 7.624\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m31.754 54.376 13.191-7.616M31.755 51.56l10.751-6.207\"/\u003e\u003c/g\u003e\u003cpath d=\"m44.94 31.52.005 15.24M18.554 31.512l-11.679-6.74\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M60.393 8.662q0 .756-.256 1.327-.256.566-.756.881t-1.244.316q-.756 0-1.262-.316-.506-.315-.756-.887-.245-.571-.245-1.333 0-.75.245-1.31.25-.566.756-.881t1.274-.316q.732 0 1.232.316.5.31.756.875.256.566.256 1.328m-3.864 0q0 .922.387 1.458.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.458 0-.929-.387-1.453-.381-.524-1.208-.524-.834 0-1.227.524t-.393 1.453\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M86.459 26.342h-.721l-2.619-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.054h.03l-.018-.327-.024-.476q-.006-.262-.006-.483v-2.768h.578zM90.765 26.342h-.619v-2.286h-2.512v2.286h-.614v-4.9h.614v2.072h2.512v-2.072h.619z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#1ff01f\" stroke=\"none\" d=\"M2.906 22.083q-.786 0-1.239.529-.452.524-.452 1.447 0 .911.417 1.447.422.529 1.268.529.321 0 .607-.053.291-.06.565-.143v.536q-.274.101-.565.149-.292.053-.697.053-.744 0-1.25-.309-.5-.31-.75-.876-.25-.571-.25-1.339 0-.744.268-1.31.274-.565.804-.881.529-.321 1.279-.321.78 0 1.352.286l-.244.523q-.226-.101-.506-.184-.274-.083-.607-.083m2.756 4.423h-.601v-5.215h.601z\" class=\"atom\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m58.133 12.586-.001 5.659M61.411 6.77l4.959-2.866\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"M84.519 20.042v-5.695M81.365 25.714l-5.021 2.902\" class=\"hi\"/\u003e\u003cpath stroke=\"#1ff01f\" d=\"m6.875 24.772 5.839 3.37\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"3-Chlorophenmetrazine","UNII":"B6P88Q2VW5","Wikidata":"Q108530213","Wikipedia":"3-Chlorophenmetrazine","XLogP":2}