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CAS 131878-23-4

(3R)-(+)-1-Benzyl-3-(tert-butoxycarbonylamino)pyrrolidine TCI B1932

(3R)-(+)-1-Benzyl-3-(tert-butoxycarbonylamino)pyrrolidine TCI B1932

Chemical Identity

CAS No.
131878-23-4
PubChem
CID 10286119·SID 87564816
Formula
C16H24N2O2
Molecular weight
276.37 g/mol
Purity
>98.0%(GC)(T)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
tert-butyl N-[(3R)-1-benzylpyrrolidin-3-yl]carbamate
SMILES
CC(C)(C)OC(=O)N[C@@H]1CCN(C1)CC2=CC=CC=C2
InChIKey
PHOIDJGLYWEUEK-CQSZACIVSA-N
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(3R)-(+)-1-Benzyl-3-(tert-butoxycarbonylamino)pyrrolidine is a chiral building block widely used in asymmetric synthesis to construct complex molecular structures. This compound plays a crucial role in organic chemistry laboratories, particularly in the development of chiral compounds with specific biological activities. Its unique stereochemistry makes it an essential tool for researchers aiming to produce enantiomerically pure substances. Due to its optical activity, it is especially valuable in pharmaceutical and biochemical research where precision is critical.

The compound's chiral nature and the presence of the tert-butoxycarbonyl (Boc) group make it a preferred choice for controlled deprotection reactions. This feature allows for multi-step synthesis strategies, enhancing the efficiency of complex molecule production. Its stability under standard laboratory conditions also contributes to its reliability in various synthetic processes. The combination of its structural specificity and functional versatility makes it a go-to reagent for advanced chemical applications.

In Indonesian laboratories, this compound is commonly used by chemists and pharmacologists in the development of new bioactive compounds. It is particularly relevant in research focused on drug discovery, active compound synthesis, and health product innovation. Its role in creating precise molecular structures supports the advancement of scientific studies in both academic and industrial settings.

TCI brochures (PDF)

  • Asymmetric synthesis: This compound is ideal for creating enantiomerically pure compounds due to its chiral structure and optical activity.
  • Chiral compound development: Its Boc group enables controlled deprotection, making it suitable for multi-step synthesis strategies.
  • Pharmaceutical research: Used in the synthesis of bioactive molecules with specific therapeutic applications.
  • Organic chemistry studies: Widely applied in research focused on molecular structure and functional group manipulation.
  • Biochemical applications: Its stereochemical properties make it valuable in studies involving enzyme interactions and biological activity.

Brand TCI
CAS number 131878-23-4
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 supplier packaging
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 stability and effectiveness. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its chemical integrity. In laboratory settings, proper ventilation should be ensured when handling the compound to minimize any potential inhalation risks. Always wear appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe handling. The compound should be kept in a secure location, away from incompatible materials to prevent any chemical interactions. Regular monitoring of storage conditions is essential to maintain the quality and usability of the material.

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