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Catalog Number:
15572
CAS Number:
755749-11-2
Acide S -3-amino-3-(2-trifluorométhylphényl)propionique
Purity:
≥ 99 % (HPLC)
Synonym(s):
L-β-Phe(2-CF3)-OH, ( S -2-Trifluorométhyl-β-phénylalanine, H-β-Phe(2-CF3)-OH
Documents
$43.87 /100 mg
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Product Information

(S)-3-Amino-3-(2-trifluoromethylphenyl)propionic acid is a versatile compound known for its unique trifluoromethyl group, which enhances its biological activity and solubility. This amino acid derivative is particularly valuable in pharmaceutical research, where it serves as a building block for the synthesis of various bioactive molecules. Its structural characteristics make it an ideal candidate for developing novel therapeutic agents, especially in the fields of neuropharmacology and medicinal chemistry. Researchers have utilized this compound in studies aimed at understanding receptor interactions and enzyme activity, showcasing its relevance in drug discovery and development.

In addition to its applications in pharmaceuticals, (S)-3-Amino-3-(2-trifluoromethylphenyl)propionic acid can also be employed in agrochemical formulations and materials science, where its properties can contribute to the development of innovative solutions. The trifluoromethyl moiety not only improves the compound's metabolic stability but also enhances its lipophilicity, making it a promising candidate for various applications. With its unique features and potential, this compound stands out as a valuable resource for researchers and industry professionals seeking to advance their projects.

Synonyms
L-β-Phe(2-CF3)-OH, ( S -2-Trifluorométhyl-β-phénylalanine, H-β-Phe(2-CF3)-OH
CAS Number
755749-11-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C 10 H 10 F 3 NON 2
Molecular Weight
233.19
MDL Number
MFCD04113683
PubChem ID
5146563
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 25 = -7,1 ± 2º (C = 1, 80 % dans AcOH)
Conditions
Conserver à 0-8°C
General Information
Synonyms
L-β-Phe(2-CF3)-OH, ( S -2-Trifluorométhyl-β-phénylalanine, H-β-Phe(2-CF3)-OH
CAS Number
755749-11-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C 10 H 10 F 3 NON 2
Molecular Weight
233.19
MDL Number
MFCD04113683
PubChem ID
5146563
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 25 = -7,1 ± 2º (C = 1, 80 % dans AcOH)
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

(S)-3-Amino-3-(2-trifluoromethylphenyl)propionic acid 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 due to its ability to modulate neurotransmitter activity.
  • Biochemical Research: It is used in studies exploring amino acid metabolism and protein synthesis, helping researchers understand cellular processes and develop new therapeutic strategies.
  • Material Science: The compound finds applications in creating advanced materials, such as polymers and coatings, that require specific chemical properties, enhancing durability and resistance to environmental factors.
  • Agricultural Chemistry: It can be utilized in the formulation of agrochemicals, contributing to the development of more effective herbicides and pesticides that minimize environmental impact while maximizing crop yield.
  • Diagnostic Tools: This chemical is also explored in the design of diagnostic agents for imaging techniques, improving the accuracy of medical diagnostics and patient outcomes.

Citations