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Catalog Number:
29615
CAS Number:
181128-25-6
S-Boc-2-amino-4,4,4-trifluoro-butyric acid
Purity:
≥ 98% (HPLC)
Documents
$148.22 /100MG
Pack Size Availability Price
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Product Information

(S)-Boc-2-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 building block for the synthesis of various bioactive molecules. Its unique structure allows for the development of potent inhibitors and modulators in drug discovery, particularly in the design of peptide-based therapeutics.

Researchers appreciate (S)-Boc-2-amino-4,4,4-trifluoro-butyric acid for its ability to facilitate the formation of peptide bonds in solid-phase peptide synthesis, streamlining the production of complex peptides. Additionally, its Boc (tert-butyloxycarbonyl) protecting group provides ease of handling and purification, making it ideal for laboratory applications. The compound's trifluoromethyl group also imparts unique electronic properties, which can be leveraged in the development of novel compounds with enhanced pharmacological profiles.

CAS Number
181128-25-6
Purity
≥ 98% (HPLC)
Molecular Formula
C9H14F3NO4
Molecular Weight
257.21
MDL Number
MFCD08532484
PubChem ID
12098057
Appearance
White to off-white powder
Optical Rotation
[a]D20 = -35 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
CAS Number
181128-25-6
Purity
≥ 98% (HPLC)
Molecular Formula
C9H14F3NO4
Molecular Weight
257.21
MDL Number
MFCD08532484
PubChem ID
12098057
Appearance
White to off-white powder
Optical Rotation
[a]D20 = -35 ± 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-2-amino-4,4,4-trifluoro-butyric acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the pharmaceutical industry, where it helps create compounds with enhanced stability and bioactivity.
  • Drug Development: Its unique trifluoromethyl group contributes to the development of novel drugs, offering improved pharmacokinetic properties and potentially leading to more effective therapies.
  • Bioconjugation: The chemical is used in bioconjugation processes, allowing researchers to attach biomolecules to drugs or imaging agents, which can enhance targeting and efficacy in treatments.
  • Research in Fluorinated Compounds: It plays a significant role in studies involving fluorinated compounds, which are known for their unique chemical properties and applications in various fields, including agrochemicals and materials science.
  • Analytical Chemistry: This compound is also applied in analytical chemistry for the development of new methods to detect and quantify amino acids and related compounds, improving accuracy in research and quality control.

Citations