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Catalog Number:
15937
CAS Number:
1049743-68-1
(R) -γ-(4-Trifluorometilbencil)-L-prolina·HCl
Purity:
≥ 99 % (HPLC)
Documents
$72.31 /25 mg
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Product Information

(R)-g-(4-Trifluoromethylbenzyl)-L-proline·HCl is a specialized amino acid derivative that has garnered attention in pharmaceutical and biochemical research. This compound is particularly valued for its role as a building block in the synthesis of peptide-based drugs and as a chiral auxiliary in asymmetric synthesis. Its unique trifluoromethyl group enhances lipophilicity, making it an attractive candidate for drug design, especially in the development of compounds targeting central nervous system disorders. Researchers have utilized this compound in various studies to explore its potential in modulating biological pathways, which could lead to innovative therapeutic strategies.

In addition to its applications in drug development, (R)-g-(4-Trifluoromethylbenzyl)-L-proline·HCl is also used in the synthesis of novel materials and catalysts, showcasing its versatility in organic chemistry. Its ability to facilitate specific reactions while maintaining stereochemical integrity makes it a valuable tool for chemists aiming to create complex molecular architectures. With its promising properties and applications, this compound stands out as a significant asset for researchers and industry professionals seeking to advance their work in medicinal chemistry and materials science.

CAS Number
1049743-68-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C13H14F3NO2 · HCl
Molecular Weight
309.72
MDL Number
MFCD06659429
PubChem ID
53398266
Melting Point
163 - 169 ?C
Appearance
Polvo blanco
Optical Rotation
[a] 20 D = -7 ± 1 ° (C=1 en HCl 1N)
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
1049743-68-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C13H14F3NO2 · HCl
Molecular Weight
309.72
MDL Number
MFCD06659429
PubChem ID
53398266
Melting Point
163 - 169 ?C
Appearance
Polvo blanco
Optical Rotation
[a] 20 D = -7 ± 1 ° (C=1 en HCl 1N)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(R)-g-(4-Trifluoromethylbenzyl)-L-proline·HCl is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key building block in the synthesis of novel pharmaceuticals, particularly in the development of drugs targeting neurological disorders due to its structural properties that enhance bioactivity.
  • Peptide Synthesis: It is employed in the synthesis of peptides, where its unique trifluoromethyl group can improve the stability and solubility of the resulting compounds, making it valuable in drug formulation.
  • Biochemical Research: Researchers use it to study protein interactions and enzyme activities, as it can act as a potent inhibitor or modulator, providing insights into biological pathways and mechanisms.
  • Material Science: The compound finds applications in the development of advanced materials, particularly in creating polymers with enhanced thermal and chemical resistance, which are crucial in various industrial applications.
  • Analytical Chemistry: It is utilized as a standard in analytical methods, helping to calibrate instruments and validate techniques in laboratories, thereby ensuring accurate and reliable results in chemical analysis.

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