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Catalog Number:
15747
CAS Number:
1217635-13-6
Boc-(S)-a-(2-fluorobenzyl)proline
Purity:
≥ 97% (HPLC)
Documents
$147.52 /100MG
Pack Size Availability Price
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Product Information

Boc-(S)-a-(2-fluorobenzyl)proline is a valuable compound in the field of medicinal chemistry and pharmaceutical research. This amino acid derivative, characterized by its unique fluorobenzyl group, serves as a crucial building block in the synthesis of various bioactive molecules. Its structural features enhance its potential in drug design, particularly in the development of peptide-based therapeutics and inhibitors. Researchers appreciate its ability to improve the pharmacological properties of compounds, making it an essential tool for those focused on optimizing drug efficacy and selectivity.

In addition to its applications in drug development, Boc-(S)-a-(2-fluorobenzyl)proline is also utilized in the synthesis of advanced materials and as a chiral auxiliary in asymmetric synthesis. Its stability and compatibility with various reaction conditions make it a preferred choice for chemists looking to streamline their synthetic pathways. The compound's unique properties not only facilitate innovative research but also offer significant advantages over similar compounds, such as enhanced solubility and improved interaction with biological targets.

CAS Number
1217635-13-6
Purity
≥ 97% (HPLC)
Molecular Formula
C17H22FNO4
Molecular Weight
323.36
MDL Number
MFCD06659155
PubChem ID
53398105
Melting Point
154 - 160 °C
Appearance
White solid
Optical Rotation
[a]D25 = -131 ± 1 º (C=1 in MeOH)
Conditions
Store at 0 - 8 °C
General Information
CAS Number
1217635-13-6
Purity
≥ 97% (HPLC)
Molecular Formula
C17H22FNO4
Molecular Weight
323.36
MDL Number
MFCD06659155
PubChem ID
53398105
Melting Point
154 - 160 °C
Appearance
White solid
Optical Rotation
[a]D25 = -131 ± 1 º (C=1 in MeOH)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-(S)-a-(2-fluorobenzyl)proline is widely utilized in research focused on:

  • Drug Development: This compound serves as a valuable building block in the synthesis of peptide-based pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Biochemical Research: It is used in the study of protein interactions and enzyme activity, helping researchers understand complex biological processes and develop new therapeutic strategies.
  • Organic Synthesis: The compound is employed in various organic synthesis applications, providing a versatile intermediate for creating complex organic molecules with specific functional groups.
  • Chiral Catalysis: Its chiral nature makes it an important component in asymmetric synthesis, allowing for the production of enantiomerically pure compounds, which are crucial in pharmaceuticals.
  • Material Science: Researchers utilize this compound in the development of novel materials, including polymers and coatings, that require specific chemical properties and functionalities.

Citations