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Catalog Number:
29619
CAS Number:
1310680-43-3
S-Boc-3-amino-4,4,4-trifluoro-butyric acid
Purity:
≥ 97% (HPLC)
Documents
$120.88 /25MG
Pack Size Availability Price
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Product Information

(S)-Boc-3-amino-4,4,4-trifluoro-butyric acid is a versatile compound widely utilized in the fields of medicinal chemistry and pharmaceutical research. This amino acid derivative features a trifluoromethyl group, which enhances its biological activity and stability, making it an attractive candidate for drug development. The Boc (tert-butyloxycarbonyl) protecting group allows for selective reactions, facilitating the synthesis of complex molecules. Researchers have employed this compound in the design of novel therapeutics, particularly in the development of peptide-based drugs, where its unique properties can lead to improved efficacy and reduced side effects.

In addition to its applications in drug synthesis, (S)-Boc-3-amino-4,4,4-trifluoro-butyric acid serves as a valuable building block in organic synthesis. Its ability to undergo various transformations while maintaining structural integrity makes it a preferred choice for chemists seeking to create intricate molecular architectures. The trifluoromethyl group not only contributes to the compound's lipophilicity but also enhances its interaction with biological targets, paving the way for innovative solutions in pharmaceutical formulations.

CAS Number
1310680-43-3
Purity
≥ 97% (HPLC)
Molecular Formula
C9H14F3NO4
Molecular Weight
257.21
MDL Number
MFCD18762152
PubChem ID
45792556
Appearance
White powder
Optical Rotation
[a]D20 = +11 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
CAS Number
1310680-43-3
Purity
≥ 97% (HPLC)
Molecular Formula
C9H14F3NO4
Molecular Weight
257.21
MDL Number
MFCD18762152
PubChem ID
45792556
Appearance
White powder
Optical Rotation
[a]D20 = +11 ± 2º (C=1 in MeOH)
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

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

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting metabolic disorders.
  • Peptide Synthesis: It is commonly used in peptide synthesis as a protecting group for amino acids, allowing for the selective modification of peptides in drug design.
  • Fluorinated Compounds: The trifluoromethyl group enhances the biological activity and stability of compounds, making it valuable in the creation of fluorinated drugs that exhibit improved pharmacokinetics.
  • Research in Biochemistry: This chemical is utilized in biochemical research to study enzyme mechanisms and protein interactions, providing insights into metabolic pathways.
  • Material Science: Its unique properties make it useful in developing advanced materials, including coatings and polymers that require specific chemical resistance and stability.

Citations