Structure via PubChem · Public domain (PubChem)
BOHD
Sign in to saveAlso known as 4-methyl-2,5-dimethoxy-beta-hydroxyphenethylamine, 4-methyl-2,5-dimethoxy-β-hydroxyphenethylamine, 2,5-dimethoxy-β-hydroxy-4-methylphenethylamine, 2,5-dimethoxy-beta-hydroxy-4-methylphenethylamine, 2-amino-1-(2,5-dimethoxy-4-methylphenyl)ethanol, 2-amino-1-(2,5-dimethoxy-4-methylphenyl)ethan-1-ol
chemical compound
In the Vinony graph
Vinony's link graph records 7 inbound references to BOHD, and connects out to 2C-G, D-methamphetamine and pharmacodynamics.
It sits within the topics Antihypertensive agents, BOx (psychedelics) and Chemical pages without DrugBank identifier.
Vinony links it to 6 Wikipedia language editions.
Chemical data
- Formula
- C11H17NO3
- Molecular weight
- 211.26 g/mol
- IUPAC name
- 2-amino-1-(2,5-dimethoxy-4-methylphenyl)ethanol
- SMILES
- CC1=CC(=C(C=C1OC)C(CN)O)OC
- InChIKey
- WCURBUJUIMRCCJ-UHFFFAOYSA-N
- XLogP
- 0.4
- Polar surface area
- 64.7 Ų
- H-bond donors
- 2
- H-bond acceptors
- 4
- Formal charge
- 0
via PubChem
Wikidata facts
- Subclass of
- phenethylamine
- Has part
- oxygen
- Mass
- 211.121
Show 6 more facts
- chemical formula
- C₁₁H₁₇NO₃
- canonical SMILES
- CC1=CC(=C(C=C1OC)C(CN)O)OC
- discoverer or inventor
- Alexander Shulgin
- described by source
- Phenethylamines I Have Known And Loved
- main regulatory text
- Misuse of Drugs Act 1971
- subject has role
- psychedelic drug
Sources (2)
via Wikidata · CC0
Connections
2C-G
Entity
D-methamphetamine
Entity
pharmacodynamics
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benzylamine
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phenethylamine
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levonordefrin
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(RS)-4-hydroxyamphetamine
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Misuse of Drugs Act 1971
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1,2,3,4-tetrahydronaphthalen-2-amine
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4-bromomethcathinone
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phenylethylpyrrolidine
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United States
Country
Canada
Country
International Standard Book Number
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drug
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digital object identifier
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epinephrine
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dopamine
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