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Catalog Number:
15934
CAS Number:
957311-13-6
Boc- (R) -γ-(2-trifluorométhylbenzyl)-L-proline
Purity:
≥ 98%
Documents
$72.31 /25 mg
Taille
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Product Information

Boc-(R)-g-(2-trifluoromethylbenzyl)-L-proline is a versatile compound widely utilized in pharmaceutical and chemical research. This protected amino acid derivative features a trifluoromethyl group, which enhances its biological activity and solubility, making it an excellent candidate for drug development and peptide synthesis. Its unique structure allows for the introduction of specific functionalities in peptide chains, facilitating the design of novel therapeutics with improved efficacy and selectivity.

Researchers appreciate Boc-(R)-g-(2-trifluoromethylbenzyl)-L-proline for its ability to serve as a building block in the synthesis of complex molecules, particularly in the development of inhibitors and modulators in medicinal chemistry. Its stability under various conditions and compatibility with standard coupling reagents make it an ideal choice for both academic and industrial applications. This compound is particularly valuable in the synthesis of bioactive peptides, where precision and functionality are paramount.

CAS Number
957311-13-6
Purity
≥ 98%
Molecular Formula
C 18 H 22 F 3 NON 4
Molecular Weight
373.37
MDL Number
MFCD06659426
PubChem ID
53398263
Melting Point
115 - 121 °C
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = -53,3 ± 2 º (C = 1 en DCM)
Conditions
Conserver à 0 - 8 °C
General Information
CAS Number
957311-13-6
Purity
≥ 98%
Molecular Formula
C 18 H 22 F 3 NON 4
Molecular Weight
373.37
MDL Number
MFCD06659426
PubChem ID
53398263
Melting Point
115 - 121 °C
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = -53,3 ± 2 º (C = 1 en DCM)
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-(R)-g-(2-trifluoromethylbenzyl)-L-proline is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the pharmaceutical industry where custom peptides are essential for drug development.
  • Drug Discovery: Its unique structural properties make it valuable in the design of novel therapeutic agents, especially in targeting specific biological pathways.
  • Bioconjugation: The compound can be used in bioconjugation processes to attach drugs or imaging agents to biomolecules, enhancing their efficacy and targeting capabilities.
  • Research in Neuroscience: It plays a role in studying receptor interactions and signaling pathways, contributing to advancements in understanding neurological disorders.
  • Fluorinated Compound Applications: The trifluoromethyl group enhances the compound's metabolic stability and bioavailability, making it particularly useful in medicinal chemistry compared to non-fluorinated analogs.

Citations