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Catalog Number:
15982
CAS Number:
221142-28-5
Boc-(±)-trans-4-phenylpyrrolidine-3-carboxylic acid
Purity:
≥ 95% (HPLC)
Synonym(s):
Boc-trans-DL-β-Pro-4-(phenyl)-OH
Documents
$58.39 /100MG
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Product Information

Boc-(±)-trans-4-phenylpyrrolidine-3-carboxylic acid is a versatile compound widely utilized in the field of organic synthesis and pharmaceutical research. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which is essential for the selective functionalization of amines in peptide synthesis and other organic reactions. Its unique structure allows for the efficient synthesis of various bioactive molecules, making it a valuable intermediate in the development of new pharmaceuticals. Researchers appreciate its stability under a range of conditions, which facilitates its use in complex synthetic pathways.

In addition to its role in synthetic chemistry, Boc-(±)-trans-4-phenylpyrrolidine-3-carboxylic acid has shown potential in the development of chiral ligands and catalysts, enhancing the efficiency of asymmetric synthesis. Its application in the synthesis of novel compounds for medicinal chemistry underscores its importance in drug discovery. With its favorable properties and broad applicability, this compound is an essential tool for chemists and researchers aiming to innovate in the fields of drug development and organic synthesis.

Synonyms
Boc-trans-DL-β-Pro-4-(phenyl)-OH
CAS Number
221142-28-5
Purity
≥ 95% (HPLC)
Molecular Formula
C16H21NO4
Molecular Weight
291.35
MDL Number
MFCD02089475
PubChem ID
3735253
Appearance
White powder
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-trans-DL-β-Pro-4-(phenyl)-OH
CAS Number
221142-28-5
Purity
≥ 95% (HPLC)
Molecular Formula
C16H21NO4
Molecular Weight
291.35
MDL Number
MFCD02089475
PubChem ID
3735253
Appearance
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-(±)-trans-4-phenylpyrrolidine-3-carboxylic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of various pharmaceutical agents, particularly in the development of drugs targeting neurological disorders.
  • Peptide Synthesis: It is commonly used in solid-phase peptide synthesis, providing a protective group that enhances the stability and yield of peptide chains.
  • Chiral Auxiliary: The compound acts as a chiral auxiliary in asymmetric synthesis, allowing chemists to produce enantiomerically pure compounds more efficiently.
  • Research in Organic Chemistry: It is employed in organic synthesis research, where its unique structure aids in the exploration of new reaction pathways and mechanisms.
  • Material Science: The compound finds applications in the development of novel materials, particularly in creating polymers with specific properties for use in various industrial applications.

Citations