Anhalidine | |
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Salts [] | |
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Anhalidine hydrochloride | |
Molecular structure via molpic | |
Conformer structure via 3Dmol.js | |
Molecular formula | C12H17NO3[1] |
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Molecular mass | 223.27 g/mol[1] |
Predicted LogP | 1.4[1] |
Chirality | achiral[2] |
Identifiers [] | |
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IUPAC name | 6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-8-ol[1] |
SMILES | CN1CCC2=CC(=C(C(=C2C1)O)OC)OC[1] |
InChI | InChI=1S/C12H17NO3/c1-13-5-4-8-6-10(15-2)12(16-3)11(14)9(8)7-13/h6,14H,4-5,7H2,1-3H3[1] |
InChIKey | DTXOXOHMRGAFDX-UHFFFAOYSA-N[1] |
Dosing |
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Anhalidine
Anhalidine (also known as 8-Isoquinolinol, 1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-, 1,2,3,4-Tetrahydro-6,7-dimethoxy-2-methyl-8-isoquinolinol or dtxoxohmrgafdx-uhfffaoysa-n) is a substance of the phenethylamine class.
Chemistry
Anhalidine is typically found in the form of its hydrochloride salt.
Stereochemistry
Anhalidine is a achiral mixture
See also
External links
- Anhalidine (Wikipedia)
- Anhalidine (Wikidata)
- Anhalidine (PubChem)
- Anhalidine (Common Chemistry)
- Anhalidine (UNII)
- Anhalidine (EPA DSSTox)
References
National Center for Biotechnology Information. PubChem Compound Summary for CID 2752318, Anhalidine. Accessed June 17, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/2752318.
U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Anhalidine. UNII: 4E6N7C369C. Global Substance Registration System. Accessed June 17, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/4E6N7C369C