C5H11NO
101.15 g/mol
Research ReagentDanger
Rac-(1R,2R)-2-aminocyclopentan-1-ol
CAS68327-03-7EC815-935-7
Category
Research Reagent
Compound Class
Amine
Primary Use
Research Compound
This compound is a stereochemically defined aminocyclopentanol bearing both an alcohol and an amine functional group on a five-membered ring. It is primarily utilized as a research reagent in laboratory settings for synthetic and investigational purposes.
research reagent for chemical synthesislaboratory intermediate in stereochemical studies
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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CAS 68327-03-7
Related Compounds
StrongSame Parent
Trans-2-Aminocyclopentanol hydrochloride
CAS68327-11-7
pharmaceutical intermediate
StrongStructure SimilarSimilarity 0.88
(1S,2S)-(+)-2-Aminocyclohexanol hydrochloride
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pharmaceutical intermediate
StrongStructure SimilarSimilarity 0.88
Trans-2-Aminocyclohexanol hydrochloride
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pharmaceutical intermediate
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Referencestereoisomer of
(1S,2S)-trans-2-Aminocyclopentanol hydrochloride
CAS68327-04-8
pharmaceutical intermediate
Safety Reference
Danger
H314Causes severe skin burns and eye damage
Identifiers
IUPAC Name
trans-(1R,2R)-2-aminocyclopentan-1-ol
InChIKey
JFFOUICIRBXFRC-RFZPGFLSSA-N
SMILES
C1C[C@H]([C@@H](C1)O)N
Synonyms (9)
- (1R,2R)-2-Aminocyclopentanol
- (R,R)-2-aminocyclopentanol
- trans 2-aminocyclopentanol