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Catalog Number:
16843
CAS Number:
922178-94-7
Boc-(S-3-amino-4-(2,4,5-trifluorophenyl)butyric acid
Purity:
≥ 98% (HPLC)
Documents
$181.67 /100MG
Pack Size Availability Price
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Product Information

Boc-(S)-3-amino-4-(2,4,5-trifluorophenyl)butyric acid is a versatile compound widely recognized for its applications in pharmaceutical research and development. This amino acid derivative, characterized by its Boc (tert-butyloxycarbonyl) protective group, serves as a crucial building block in the synthesis of peptide-based therapeutics. Its unique trifluorophenyl moiety enhances lipophilicity and biological activity, making it particularly valuable in the design of potent drug candidates targeting various diseases, including cancer and neurological disorders.

Researchers appreciate the compound's stability and ease of handling, which facilitate its incorporation into complex molecular architectures. Its ability to modulate biological pathways through selective receptor interactions positions it as a promising candidate in medicinal chemistry. Additionally, Boc-(S)-3-amino-4-(2,4,5-trifluorophenyl)butyric acid's favorable pharmacokinetic properties make it an attractive option for developing novel therapeutics, providing a competitive edge over similar compounds in the market.

CAS Number
922178-94-7
Purity
≥ 98% (HPLC)
Molecular Formula
C15H18F3NO4
Molecular Weight
333.3
MDL Number
MFCD06659150
PubChem ID
21911205
Melting Point
130-136 °C
Appearance
White powder
Optical Rotation
[a]D25 = -14 ± 2º (C=1 in EtOH)
Conditions
Store at 0-8°C
General Information
CAS Number
922178-94-7
Purity
≥ 98% (HPLC)
Molecular Formula
C15H18F3NO4
Molecular Weight
333.3
MDL Number
MFCD06659150
PubChem ID
21911205
Melting Point
130-136 °C
Appearance
White powder
Optical Rotation
[a]D25 = -14 ± 2º (C=1 in EtOH)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-(S)-3-amino-4-(2,4,5-trifluorophenyl)butyric acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a crucial intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Peptide Synthesis: It is commonly used in the synthesis of peptides, where its protective Boc group allows for selective reactions, enhancing the efficiency of peptide assembly.
  • Research in Medicinal Chemistry: Researchers leverage its unique trifluorophenyl group to explore structure-activity relationships in drug design, potentially leading to more effective therapeutic agents.
  • Biochemical Studies: The compound's ability to modulate biological pathways makes it valuable in biochemical assays, helping scientists understand disease mechanisms and drug interactions.
  • Material Science: Its properties are explored in the development of novel materials, particularly those requiring specific chemical functionalities for advanced applications.

Citations