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Home/Compounds/Research Reagent/(1S,2S)-2-Aminocyclohexanol
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

Harmful
Harmful
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-