(3R)-(-)-1-Benzyl-3-aminopyrrolidine TCI A1173

Chemical Identity

CAS No.: 114715-39-8
PubChem: CID 1519354·SID 87562651
Formula: C11H16N2
Molecular weight: 176.26 g/mol
Purity: >98.0%(GC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

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

Rp 900.900,00

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(3R)-(-)-1-Benzyl-3-aminopyrrolidine is a chiral compound widely used in asymmetric synthesis to construct complex molecular structures. This material plays a crucial role in organic chemistry laboratories, where it serves as a key building block for the synthesis of enantiomerically pure compounds. Its chiral nature allows for precise control over reaction pathways, making it essential in the development of pharmaceuticals and bioactive molecules. Due to its specific stereochemistry, it is particularly valuable in applications requiring high selectivity and efficiency in synthetic processes.

The compound is known for its chemical stability under normal conditions, although it is sensitive to temperature and humidity changes. Its unique chiral configuration enables chemists to direct reactions with greater accuracy, enhancing the overall efficiency of synthetic procedures. This characteristic makes it a preferred choice for researchers aiming to achieve high-purity products in both academic and industrial settings. Additionally, its reliability and reproducibility contribute to its widespread use in laboratory environments.

In Indonesian laboratories, (3R)-(-)-1-Benzyl-3-aminopyrrolidine is commonly employed in research focused on organic synthesis and pharmacology. It is a vital component in the development of new therapeutic agents and is frequently used in both fundamental and applied chemical studies. Its presence in research institutions and universities underscores its importance in advancing scientific knowledge and innovation in the field of chemistry.

TCI brochures (PDF)

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

Related TCI products

Organic synthesis research utilizes this compound to create enantiomerically pure compounds essential for pharmaceutical development.
Pharmacological studies benefit from its chiral structure, enabling the synthesis of bioactive molecules with specific therapeutic properties.
Asymmetric catalysis applications rely on its stereochemical properties to direct reactions with high selectivity and efficiency.
Drug discovery programs use it to develop new compounds with potential medical applications and improved biological activity.
Academic research in chemistry employs it as a key reagent for exploring complex molecular architectures and reaction mechanisms.

Brand	TCI
CAS number	114715-39-8
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid (as per standard product description)
Storage	Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to minimize exposure to moisture and temperature fluctuations. Due to its sensitivity to environmental conditions, it is important to handle it with care during storage and use. Proper labeling of containers is essential to ensure safe handling and prevent cross-contamination. In laboratory settings, it should be kept away from incompatible materials and stored in a designated chemical storage area. Regular monitoring of storage conditions is advised to maintain the integrity of the compound throughout its shelf life.

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