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Catalog Number:
29618
CAS Number:
1310680-29-5
Acide R -Boc-3-amino-4,4,4-trifluoro-butyrique
Purity:
≥ 98 % (HPLC)
Documents
$120.88 /25 mg
Taille
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Product Information

(R)-Boc-3-amino-4,4,4-trifluoro-butyric acid is a specialized amino acid derivative that plays a significant role in peptide synthesis and pharmaceutical research. This compound features a trifluoromethyl group, which enhances its biological activity and stability, making it an attractive choice for researchers focused on developing novel therapeutics. Its Boc (tert-butyloxycarbonyl) protecting group allows for selective deprotection, facilitating the synthesis of complex peptides with high purity and yield.

In the pharmaceutical industry, (R)-Boc-3-amino-4,4,4-trifluoro-butyric acid is utilized in the design of bioactive compounds, particularly in the development of inhibitors and modulators for various biological pathways. Its unique properties enable researchers to explore innovative applications in drug discovery, particularly in areas targeting metabolic disorders and cancer therapies. By incorporating this compound into their research, scientists can leverage its distinct characteristics to enhance the efficacy and specificity of their therapeutic candidates.

CAS Number
1310680-29-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C 9 H 14 F 3 NON 4
Molecular Weight
257.21
MDL Number
MFCD18762150
PubChem ID
45792556
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = -12 ± 2º (C=1 dans MeOH)
Conditions
Conserver à 0-8 °C
General Information
CAS Number
1310680-29-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C 9 H 14 F 3 NON 4
Molecular Weight
257.21
MDL Number
MFCD18762150
PubChem ID
45792556
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = -12 ± 2º (C=1 dans MeOH)
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

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

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting metabolic disorders due to its unique trifluoromethyl group, which enhances bioactivity.
  • Peptide Synthesis: It is employed in the production of peptides, providing a protective group that facilitates the selective modification of amino acids, making it easier for researchers to create complex peptide structures.
  • Fluorinated Compound Research: The trifluoromethyl moiety allows for the exploration of new fluorinated compounds, which are often more stable and exhibit unique properties, making them valuable in drug design and materials science.
  • Analytical Chemistry: This compound can be used as a standard in analytical methods, helping researchers to calibrate instruments and validate results when analyzing similar fluorinated compounds.
  • Bioconjugation Applications: Its functional groups enable bioconjugation processes, allowing for the attachment of biomolecules to surfaces or other compounds, which is crucial in developing targeted drug delivery systems.

Citations