C6H13NO
115.17 g/mol
Research ReagentWarning
(1S,2S)-2-AMINOCYCLOHEXANOL
CAS74111-21-0EC625-678-0
Category
Research Reagent
Compound Class
Amine
Primary Use
Research Compound
(1S,2S)-2-aminocyclohexanol is a chiral organic compound with a trans-configured amine and alcohol group on a cyclohexane ring. It is primarily used as a research compound in chemical and pharmaceutical studies.
research compoundlaboratory reagent
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
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Related Compounds
StrongSame Parent
(1S,2S)-(+)-2-Aminocyclohexanol hydrochloride
CAS13374-30-6
pharmaceutical intermediate
StrongStructure SimilarSimilarity 0.88
(1S,2S)-trans-2-Aminocyclopentanol hydrochloride
CAS68327-04-8
pharmaceutical intermediate
StrongStructure SimilarSimilarity 0.88
Trans-2-Aminocyclopentanol hydrochloride
CAS68327-11-7
pharmaceutical intermediate
ReferenceSame Category
N,N'-disuccinimidyl carbonate
CAS74124-79-1
research compound
ReferenceSame Category
AMP-PCP (disodium)
CAS7414-56-4
research compound
ReferenceSame Category
N-(2-Acetamido)iminodiacetic acid monosodium salt
CAS7415-22-7
research compound
ReferenceSame Category
Guanosine-5'-diphosphate disodium salt
CAS7415-69-2
research compound
Referencestereoisomer of
(R)-2-Aminocyclohenanol
CAS931-16-8
pharmaceutical intermediate
Safety Reference
Warning
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
Identifiers
IUPAC Name
trans-(1S,2S)-2-aminocyclohexan-1-ol
InChIKey
PQMCFTMVQORYJC-WDSKDSINSA-N
SMILES
C1CC[C@@H]([C@H](C1)N)O
Synonyms (10)
- (1S,2S)-2-AMINOCYCLOHEXANOL
- (S,S)-2-aminocyclohexanol
- 2-Aminocyclohexanol, (E)-
- Cyclohexanol,2-amino-,trans-
Sourcing (1S,2S)-2-AMINOCYCLOHEXANOL?
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