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Catalog Number:
14283
CAS Number:
190897-47-3
( S )-Boc-β 2 -HomoAla-OH
Purity:
≥ 98 % (TLC)
Synonym(s):
Ácido ( S )-3-(Boc-amino)-2-metilpropiónico
Documents
$186.78 /100 mg
Tamaño
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Product Information

(S)-Boc-b2-HomoAla-OH is a valuable compound widely utilized in the field of peptide synthesis and pharmaceutical research. This amino acid derivative, characterized by its Boc (tert-butyloxycarbonyl) protecting group, offers enhanced stability and ease of handling during chemical reactions. Its unique structure allows for the incorporation of non-natural amino acids into peptides, making it an essential building block for researchers developing novel therapeutics and biologically active compounds.

In the pharmaceutical industry, (S)-Boc-b2-HomoAla-OH is particularly beneficial for the synthesis of peptide-based drugs, where it can improve the bioavailability and efficacy of therapeutic agents. Its application extends to the development of targeted drug delivery systems and the creation of peptide libraries for high-throughput screening. Researchers appreciate its compatibility with various coupling reagents and its ability to facilitate the formation of complex peptide structures, thereby streamlining the synthesis process and enhancing productivity in laboratory settings.

Synonyms
Ácido ( S )-3-(Boc-amino)-2-metilpropiónico
CAS Number
190897-47-3
Purity
≥ 98 % (TLC)
Molecular Formula
C9H17Nº4
Molecular Weight
203.3
MDL Number
MFCD04040045
PubChem ID
4192640
Appearance
Polvo blanco
Optical Rotation
[a] D 25 = 19 ± 2 º (C=1 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido ( S )-3-(Boc-amino)-2-metilpropiónico
CAS Number
190897-47-3
Purity
≥ 98 % (TLC)
Molecular Formula
C9H17Nº4
Molecular Weight
203.3
MDL Number
MFCD04040045
PubChem ID
4192640
Appearance
Polvo blanco
Optical Rotation
[a] D 25 = 19 ± 2 º (C=1 en MeOH)
Conditions
Conservar entre 0 y 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-b2-HomoAla-OH 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 development of pharmaceutical compounds. Its protective Boc group allows for selective reactions, enhancing the efficiency of peptide assembly.
  • Drug Development: In medicinal chemistry, it is used to create novel drug candidates that target specific biological pathways. Its structural properties enable the design of compounds with improved bioactivity and reduced side effects.
  • Biotechnology: This chemical plays a crucial role in the production of biologically active molecules, including enzymes and hormones. Its application in recombinant DNA technology facilitates the creation of proteins with desired characteristics.
  • Research in Neuroscience: Researchers utilize this compound to study neuropeptides, contributing to the understanding of neurological disorders. Its ability to mimic natural amino acids makes it a useful tool in exploring receptor interactions.
  • Cosmetic Formulations: The compound is also being explored in cosmetic chemistry for its potential in developing anti-aging products. Its properties can enhance skin penetration and improve the efficacy of active ingredients.

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