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Catalog Number:
15721
CAS Number:
113756-89-1
Ácido Boc-L-2-amino-5-fenilpentanoico·DCHA
Purity:
≥ 98%
Synonym(s):
Boc-L-Nva(5-fenil)-OH·DCHA, Boc-Nva(5-fenil)-OH·DCHA
Documents
$58.39 /100 mg
Tamaño
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Product Information

Boc-L-2-amino-5-phenylpentanoic acid·DCHA is a valuable compound widely utilized in peptide synthesis and pharmaceutical research. This amino acid derivative features a tert-butyloxycarbonyl (Boc) protecting group, which enhances its stability and reactivity during chemical reactions. Its unique structure allows for the incorporation of phenyl and branched alkyl groups, making it an ideal candidate for developing complex peptides and biologically active molecules. Researchers appreciate its role in the synthesis of peptide-based drugs, where precise control over amino acid sequences is crucial for therapeutic efficacy.

In addition to its applications in drug development, Boc-L-2-amino-5-phenylpentanoic acid·DCHA serves as a versatile building block in the synthesis of various bioactive compounds. Its favorable solubility and compatibility with standard coupling reagents make it a preferred choice for chemists looking to streamline their synthetic processes. With its ability to facilitate the creation of novel peptides, this compound holds significant potential in advancing medicinal chemistry and biopharmaceuticals, making it an essential addition to any research laboratory focused on peptide synthesis.

Synonyms
Boc-L-Nva(5-fenil)-OH·DCHA, Boc-Nva(5-fenil)-OH·DCHA
CAS Number
113756-89-1
Purity
≥ 98%
Molecular Formula
C28H46N2O4
Molecular Weight
474.68
MDL Number
MFCD06410979
PubChem ID
13876149
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-L-Nva(5-fenil)-OH·DCHA, Boc-Nva(5-fenil)-OH·DCHA
CAS Number
113756-89-1
Purity
≥ 98%
Molecular Formula
C28H46N2O4
Molecular Weight
474.68
MDL Number
MFCD06410979
PubChem ID
13876149
Appearance
Polvo blanco
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

Boc-L-2-amino-5-phenylpentanoic acid·DCHA is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the pharmaceutical industry, where it aids in developing new drugs with enhanced efficacy.
  • Drug Development: Its unique structure allows for the modification of drug candidates, improving their bioavailability and stability, which is crucial in the development of effective therapeutic agents.
  • Biochemical Research: Researchers use this compound to study protein interactions and enzyme activities, helping to uncover mechanisms of action in various biological processes.
  • Cosmetic Formulations: The compound can be incorporated into cosmetic products for its potential skin benefits, such as enhancing skin hydration and elasticity.
  • Academic Research: It is often used in academic laboratories for teaching purposes, providing students with hands-on experience in organic synthesis and analytical techniques.

Citas