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Catalog Number:
17854
CAS Number:
161659-80-9
S-1-Benzyl-pyrrolidine-3-carboxylic acid
Purity:
≥ 98%
Synonym(s):
(S-1-N-Benzyl-β-proline
Documents
$110.00 /250MG
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Product Information

(S)-1-Benzyl-pyrrolidine-3-carboxylic acid is a versatile compound with significant applications in the pharmaceutical and chemical industries. This chiral amino acid derivative is recognized for its role as a building block in the synthesis of various bioactive molecules, particularly in the development of pharmaceuticals that target central nervous system disorders. Its unique structure allows for the modulation of biological activity, making it a valuable component in drug formulation and research.

Researchers and industry professionals appreciate (S)-1-Benzyl-pyrrolidine-3-carboxylic acid for its potential in asymmetric synthesis, where it can serve as a chiral auxiliary to enhance the selectivity of reactions. Additionally, its stability and compatibility with various reaction conditions make it an ideal candidate for complex organic synthesis. The compound's ability to facilitate the creation of novel therapeutic agents underscores its importance in advancing medicinal chemistry and drug discovery.

Synonyms
(S-1-N-Benzyl-β-proline
CAS Number
161659-80-9
Purity
≥ 98%
Molecular Formula
C12H15NO2
Molecular Weight
205.26
MDL Number
MFCD04115301
PubChem ID
4617348
Appearance
Yellow to light brown solid
Conditions
Store at 0-8°C
General Information
Synonyms
(S-1-N-Benzyl-β-proline
CAS Number
161659-80-9
Purity
≥ 98%
Molecular Formula
C12H15NO2
Molecular Weight
205.26
MDL Number
MFCD04115301
PubChem ID
4617348
Appearance
Yellow to light brown solid
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-1-Benzyl-pyrrolidine-3-carboxylic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Chiral Synthesis: Its chiral nature makes it valuable in asymmetric synthesis, allowing researchers to create enantiomerically pure compounds, which are crucial in drug formulation.
  • Biochemical Research: The compound is used in studies related to protein interactions and enzyme activity, helping scientists understand biological mechanisms at a molecular level.
  • Material Science: It can be incorporated into polymer matrices to enhance the properties of materials, making it useful in developing advanced composites for various applications.
  • Flavor and Fragrance Industry: Due to its aromatic properties, it finds applications in creating unique flavors and fragrances, appealing to manufacturers in the food and cosmetics sectors.

Citations