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Catalog Number:
11662
CAS Number:
14328-51-9(net)
Trifluoroacétate de L-2-cyclohexylglycine
Purity:
≥ 99 % (CCM)
Synonym(s):
L-Chg-OH·TFA, HL-Cyclohexyl-Gly-OH·TFA, H-Chg-OH·TFA
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Product Information

L-2-Cyclohexylglycine trifluoroacetate is a versatile compound known for its unique properties and applications in various fields, particularly in pharmaceutical and biochemical research. This compound serves as an important building block in the synthesis of bioactive molecules, offering researchers a reliable option for developing new therapeutic agents. Its trifluoroacetate form enhances solubility and stability, making it ideal for use in drug formulation and delivery systems.

In addition to its role in drug development, L-2-Cyclohexylglycine trifluoroacetate is also utilized in studies related to neurotransmitter modulation and receptor interactions, providing valuable insights into neurological processes. Its ability to mimic natural amino acids allows for the exploration of new pathways in medicinal chemistry. Researchers and industry professionals can leverage this compound for innovative applications, including the design of novel pharmaceuticals and the advancement of biochemical assays.

Synonyms
L-Chg-OH·TFA, HL-Cyclohexyl-Gly-OH·TFA, H-Chg-OH·TFA
CAS Number
14328-51-9(net)
Purity
≥ 99 % (CCM)
Molecular Formula
C 8 H 15 NO 2
Molecular Weight
157.21
MDL Number
MFCD02259527
PubChem ID
224391
Appearance
Poudre blanche
Optical Rotation
[a] D 24 = +29 ± 2º (C = 1 dans HCl 1N)
Conditions
Conserver à 0-8°C
General Information
Synonyms
L-Chg-OH·TFA, HL-Cyclohexyl-Gly-OH·TFA, H-Chg-OH·TFA
CAS Number
14328-51-9(net)
Purity
≥ 99 % (CCM)
Molecular Formula
C 8 H 15 NO 2
Molecular Weight
157.21
MDL Number
MFCD02259527
PubChem ID
224391
Appearance
Poudre blanche
Optical Rotation
[a] D 24 = +29 ± 2º (C = 1 dans HCl 1N)
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

L-2-Cyclohexylglycine trifluoroacetate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a building block in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Biochemical Research: It is used in studies investigating amino acid metabolism and its effects on cellular functions, providing insights into metabolic pathways.
  • Chiral Catalysis: This chemical acts as a chiral auxiliary in asymmetric synthesis, helping researchers create enantiomerically pure compounds, which are crucial in drug formulation.
  • Analytical Chemistry: It is employed in chromatography for the separation and analysis of complex mixtures, enhancing the accuracy of analytical results.
  • Material Science: The compound is explored for its potential applications in developing novel materials with unique properties, such as improved thermal stability and mechanical strength.

Citations