(3R)-(-)-1-Benzyl-3-(ethylamino)pyrrolidine TCI B1580

Chemical Identity

CAS No.: 376591-05-8
PubChem: CID 12362913·SID 87564483
Formula: C13H20N2
Molecular weight: 204.31 g/mol
Purity: >95.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (3R)-1-benzyl-N-ethylpyrrolidin-3-amine
SMILES: CCN[C@@H]1CCN(C1)CC2=CC=CC=C2
InChIKey: ZSIUSRJKSLXIJH-CYBMUJFWSA-N

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(3R)-(-)-1-Benzyl-3-(ethylamino)pyrrolidine is a chiral compound widely used in asymmetric synthesis to construct molecules with specific optical properties. This compound plays a crucial role in organic chemistry laboratories, particularly in the development of bioactive molecules. Its unique structure, featuring a modified pyrrolidine ring with a benzyl and ethylamine group, makes it a key building block in the synthesis of pharmaceuticals and other complex organic compounds. Due to its chiral nature, it is essential for achieving stereochemical control in chemical reactions.

This compound is preferred for its well-defined chirality and its ability to participate in enantioselective reactions. Its structural complexity allows it to be a versatile tool in the hands of chemists, enabling the creation of molecules with high pharmacological activity. The compound's stability and reactivity under controlled conditions make it a reliable choice for researchers aiming to produce optically active compounds. Its use in asymmetric synthesis ensures the production of compounds with specific stereochemistry, which is critical in drug development and other advanced chemical applications.

In Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in pharmacology and the synthesis of active compounds. Local researchers rely on it for the development of new drugs and the modification of existing compounds. Its importance in the field of medicinal chemistry makes it a valuable resource for both academic and industrial research settings. The compound is also used in the study of stereoselectivity and in the design of chiral catalysts.

TCI brochures (PDF)

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

Related TCI products

Asymmetric Synthesis: This compound is ideal for creating optically active molecules due to its well-defined chirality, making it a preferred choice in enantioselective reactions.
Pharmaceutical Development: Its role in constructing bioactive molecules makes it essential for drug discovery and the synthesis of pharmaceutical compounds.
Organic Chemistry Research: Widely used in academic and industrial settings for the synthesis of complex organic structures with specific stereochemistry.
Chiral Catalyst Design: Its structural features allow it to be used in the development of chiral catalysts for selective chemical transformations.
Pharmacological Studies: It is frequently employed in research aimed at understanding the stereochemical effects of compounds on biological systems.

Brand	TCI
CAS number	376591-05-8
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid or liquid, depending on the specific formulation
Storage	Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its chiral nature, it is important to handle the compound with care to avoid any unintended racemization or loss of optical purity. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling the compound. Proper ventilation should be ensured in the workspace to minimize exposure to any potential vapors. The compound should not be stored near incompatible substances to prevent any chemical interactions that could compromise its stability or effectiveness.

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