(3S)-(+)-1-Benzyl-3-aminopyrrolidine TCI A1174

Chemical Identity

CAS No.: 114715-38-7
PubChem: CID 1519353·SID 87562652
Formula: C11H16N2
Molecular weight: 176.26 g/mol
Purity: >98.0%(GC)(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (3S)-1-benzylpyrrolidin-3-amine
SMILES: C1CN(C[C@H]1N)CC2=CC=CC=C2
InChIKey: HBVNLKQGRZPGRP-NSHDSACASA-N

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Berat 10g 25g

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(3S)-(+)-1-Benzyl-3-aminopyrrolidine is a chiral building block widely used in asymmetric synthesis to construct complex molecular structures. This compound plays a vital role in laboratories where precise control over stereochemistry is essential. Its unique stereochemical configuration makes it an indispensable tool in the development of pharmaceuticals and organic compounds. As a chiral molecule, it enables the synthesis of enantiomerically pure compounds, which are critical in drug development and biochemical research.

The compound's stability and reactivity make it a preferred choice for chemists working in both academic and industrial settings. Its ability to participate in various chemical reactions while maintaining its stereochemical integrity ensures consistent results in synthetic processes. Additionally, its well-defined structure allows for predictable outcomes in reactions, which is crucial for reproducibility in scientific research. These properties contribute to its popularity among researchers seeking reliable and efficient synthetic pathways.

In Indonesian laboratories, (3S)-(+)-1-Benzyl-3-aminopyrrolidine is commonly used in pharmaceutical and organic chemistry research. It is a key component in the synthesis of bioactive compounds and is utilized by research institutions and universities to develop new drugs and study molecular structures. Its role in creating isomers with specific biological activities makes it a valuable resource in the pursuit of innovative scientific discoveries.

TCI brochures (PDF)

Chiral Building Blocks 2025-04-14 · p. 3

Related TCI products

Asymmetric synthesis of pharmaceutical compounds due to its chiral structure and stereochemical control
Development of bioactive molecules requiring precise isomer formation for therapeutic applications
Study of stereoselective reactions to understand the impact of molecular configuration on biological activity
Preparation of enantiomerically pure compounds for drug development and pharmacological research
Investigation of molecular interactions in organic chemistry to optimize synthetic pathways

Brand	TCI
CAS number	114715-38-7
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid
Storage	Store in a cool, dry place away from light

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep it in a sealed container to prevent moisture absorption and contamination. Due to its chemical nature, it should be handled in a well-ventilated area, and appropriate personal protective equipment, such as gloves and safety goggles, should be worn. While it does not require special refrigeration, it is important to ensure that it is not exposed to incompatible substances. Proper labeling and storage conditions will help maintain its stability and effectiveness for use in laboratory applications.

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