C7H13NO
127.18 g/mol
Pharmaceutical IntermediateDanger
(R)-(-)-3-Quinuclidinol
CAS25333-42-0EC246-857-6
Category
Pharmaceutical Intermediate
Compound Class
Alcohol
Primary Use
Pharmaceutical Intermediate
This compound is a chiral bicyclic amino alcohol used as an intermediate in pharmaceutical manufacturing. Its structure features a quinuclidine ring system with a stereochemically defined alcohol group.
pharmaceutical intermediateresearch compound for organic synthesis
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 25333-42-0
Related Compounds
ReferenceSame Category
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5-Chloro-2-((tert-butoxycarbonyl)amino)benzoic acid
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pharmaceutical intermediate
Referencestereoisomer of
(+)-3-quinuclidinol
CAS34583-34-1
research compound
Referencestereoisomer of
3-quinuclidinol
CAS1619-34-7
pharmaceutical intermediate
Referencesame scaffold
Aceclidine hydrochloride
CAS6109-70-2
pharmaceutical intermediate
Referencesame scaffold
Quinuclidin-3-ylmethanol hydrochloride
CAS79221-75-3
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Safety Reference
Danger
H228Flammable solid
H302Harmful if swallowed
H314Causes severe skin burns and eye damage
H317May cause an allergic skin reaction
Identifiers
IUPAC Name
(3R)-1-azabicyclo[2.2.2]octan-3-ol
InChIKey
IVLICPVPXWEGCA-ZETCQYMHSA-N
SMILES
C1CN2CCC1[C@H](C2)O
Synonyms (27)
- Solifenacin EP Impurity E
- (1S,3R,4S)-quinuclidin-3-ol
- (3R)-3-Quinuclidinol
- (3r)-quinuclidin-3-ol
- (R)-(-)-3-Quinuclidinol
- (R)-3-Hydroxyquinuclidine
- (R)-3-Quinuclidol
- (R)-Quinuclidin-3-ol
- (R)-quinuclidine-3-ol
- 3(R)-quinuclidinol
- 3-(R)-Hydroxyquinuclidine
- 3-Quinuclidinol R isomer
- 3-Quinuclidinol l-form
- 3-Quinuclidinol, (-)-
- NARONAPRIDE METABOLITE M5
- l-3-Quinuclidinol