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CAS 6216-63-3

N-Carbobenzoxy-L-prolinol TCI C3332

N-Carbobenzoxy-L-prolinol TCI C3332

Chemical Identity

Other names
N-Cbz-L-prolinol · (S)-1-Carbobenzoxy-2-pyrrolidinemethanol · (S)-1-Cbz-2-pyrrolidinemethanol · N-Benzyloxycarbonyl-L-prolinol · (S)-1-Benzyloxycarbonyl-2-pyrrolidinemethanol
CAS No.
6216-63-3
PubChem
CID 11096562·SID 468591088
Formula
C13H17NO3
Molecular weight
235.28 g/mol
Purity
>98.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
benzyl (2S)-2-(hydroxymethyl)pyrrolidine-1-carboxylate
SMILES
C1CC(N(C1)C(=O)OCC2=CC=CC=C2)CO
InChIKey
BJTNHGVCFWDNDP-LBPRGKRZSA-N
MDL
MDL02683224
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N-Carbobenzoxy-L-prolinol (TCI C3332, CAS 6216-63-3) is a chiral building block widely used in asymmetric synthesis within laboratory settings. It serves as a key intermediate in the development of chiral molecules, which are essential in pharmaceutical and organic chemistry research. This compound is particularly valuable for its ability to maintain stereochemical integrity during complex synthetic processes. Its role in the laboratory is critical for creating molecules with specific spatial configurations, which are often required in drug development and advanced chemical research.

The compound is preferred due to its chemical stability and controlled reactivity under specific conditions. The presence of a protected carboxyl group allows for selective chemical modifications without compromising the core structure of the molecule. This feature makes it highly versatile for various synthetic transformations. Additionally, its good solubility in organic solvents enhances its usability in a wide range of chemical reactions. These properties make it a reliable and efficient choice for researchers working in asymmetric synthesis.

In Indonesian laboratories, N-Carbobenzoxy-L-prolinol is commonly used in organic chemistry research, especially in the fields of asymmetric synthesis and drug development. Its availability supports local scientific efforts in creating chiral compounds with specific biological activities. Researchers rely on this compound to advance their work in synthesizing complex molecules with precise stereochemistry, contributing to the growth of scientific innovation in the region.

TCI brochures (PDF)

  • Asymmetric synthesis of chiral compounds due to its stereochemical stability and controlled reactivity.
  • Development of pharmaceuticals requiring precise molecular configurations for drug efficacy.
  • Organic chemistry research involving selective functional group modifications in complex molecules.
  • Creation of chiral intermediates for use in advanced synthetic pathways and catalytic reactions.
  • Support for academic and industrial research in the production of bioactive molecules with specific spatial arrangements.

Brand TCI
CAS number 6216-63-3
Molecular formula —
Purity —
Category Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes —
Physical form —
Storage Store in a cool, dry place away from light and moisture

N-Carbobenzoxy-L-prolinol 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 to prevent exposure to air and humidity, which could affect its stability. General laboratory precautions include handling with care to avoid contamination and ensuring proper ventilation when working with the compound. Due to its chemical nature, it should be stored separately from incompatible substances. Proper labeling and storage conditions are essential to ensure safety and maintain the quality of the compound for research applications.

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