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Catalog Number:
15022
CAS Number:
140148-70-5
Boc-(3S-1-pyrrolidine-3-carboxylic acid
Purity:
≥ 98% (NMR)
Synonym(s):
(3S-Boc-β-Pro-OH
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Product Information

Boc-(3S)-1-pyrrolidine-3-carboxylic acid is a versatile compound widely utilized in the field of organic synthesis and pharmaceutical development. This compound, also known as Boc-3-pyrrolidinecarboxylic acid, features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and reactivity in various chemical reactions. Its unique structure allows for effective incorporation into peptide synthesis, making it an essential building block for researchers working on drug design and development.

The compound's chiral nature provides significant advantages in the synthesis of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for developing effective and safe medications. Its applications extend to the production of biologically active molecules, where it serves as a precursor in the synthesis of various pharmaceutical agents. With its favorable properties, Boc-(3S)-1-pyrrolidine-3-carboxylic acid stands out as a reliable choice for researchers seeking to enhance their synthetic pathways and improve the efficacy of their compounds.

Synonyms
(3S-Boc-β-Pro-OH
CAS Number
140148-70-5
Purity
≥ 98% (NMR)
Molecular Formula
C10H17NO4
Molecular Weight
215.25
MDL Number
MFCD03094728
PubChem ID
2760529
Appearance
White to off-white powder
Conditions
Store at 0-8°C
General Information
Synonyms
(3S-Boc-β-Pro-OH
CAS Number
140148-70-5
Purity
≥ 98% (NMR)
Molecular Formula
C10H17NO4
Molecular Weight
215.25
MDL Number
MFCD03094728
PubChem ID
2760529
Appearance
White to off-white powder
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

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

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for selective reactions and enhancing the yield of desired products.
  • Drug Development: It plays a crucial role in the design of pharmaceutical compounds, particularly in the development of drugs targeting neurological disorders due to its structural properties.
  • Organic Synthesis: Researchers use it as an intermediate in organic synthesis, facilitating the creation of complex molecules with high specificity.
  • Bioconjugation: The compound is effective in bioconjugation processes, where it helps attach biomolecules to surfaces or other compounds, improving the functionality of diagnostics and therapeutics.
  • Research in Chiral Catalysis: Its chiral nature makes it valuable in studies related to asymmetric synthesis, providing insights into reaction mechanisms and improving the efficiency of catalysis.

Citations