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Home/Compounds/Pharmaceutical Intermediate/(S)-(+)-1-Benzyl-3-aminopyrrolidine
C11H16N2
176.26 g/mol
Pharmaceutical IntermediateDanger

(3S)-(+)-1-Benzyl-3-aminopyrrolidine

CAS114715-38-7EC623-347-5
Category
Pharmaceutical Intermediate
Compound Class
Amine
Primary Use
Pharmaceutical Intermediate

This compound is a chiral amine compound used as a pharmaceutical intermediate in the synthesis of optically active molecules. Its structure features a pyrrolidine ring with a benzyl substituent and a stereochemically defined amine group.

Pharmaceutical intermediate for chiral synthesisBuilding block in asymmetric 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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Related Compounds

StrongSame Parent

(3S)-(+)-1-Benzyl-3-aminopyrrolidine dihydrochloride

CAS131852-54-5

pharmaceutical intermediate

SimilarStructure SimilarSimilarity 0.81

(R)-3-Amino-1-benzylpiperidine

CAS168466-84-0

pharmaceutical intermediate

SimilarStructure SimilarSimilarity 0.81

(S)-1-Benzyl-3-aminopiperidine

CAS168466-85-1

pharmaceutical intermediate

SimilarStructure SimilarSimilarity 0.81

1-Benzyl-3-aminopiperidine

CAS60407-35-4

pharmaceutical intermediate

SimilarStructure SimilarSimilarity 0.81

(R)-1-Benzyl-3-aminopiperidine dihydrochloride

CAS876160-18-8

pharmaceutical intermediate

ApplicationSame Use

(R)-1-Cbz-3-aminopyrrolidine

CAS122536-73-6

pharmaceutical intermediate

ApplicationSame Use

(R)-3-(Boc-amino)pyrrolidine

CAS122536-77-0

pharmaceutical intermediate

ApplicationSame Use

(S,S)-2,8-Diazabicyclo[4.3.0]nonane

CAS151213-40-0

pharmaceutical intermediate

Safety Reference

Corrosive
Corrosive
Harmful
Harmful
Danger
H314Causes severe skin burns and eye damage
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
Identifiers
IUPAC Name

(3S)-1-benzylpyrrolidin-3-amine

InChIKey

HBVNLKQGRZPGRP-NSHDSACASA-N

SMILES

C1CN(C[C@H]1N)CC2=CC=CC=C2

Synonyms (15)

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