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Catalog Number:
03941
CAS Number:
67708-97-8
Ester 4-nitrophénylique de l'acide boc-L-α-aminobutyrique
Purity:
≥ 97 % (HPLC)
Synonym(s):
Boc-L-Abu-ONp, Ester 4-nitrophénylique de l'acide boc-L-2-aminobutanoïque
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$30.35 /1G
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Product Information

Boc-L-a-aminobutyric acid 4-nitrophenyl ester is a versatile compound widely utilized in peptide synthesis and pharmaceutical research. This ester serves as a protective group for amino acids, allowing for selective reactions during the synthesis of complex peptides. Its unique structure, featuring a 4-nitrophenyl group, enhances its reactivity and makes it an excellent choice for chemists looking to streamline their synthetic pathways. The compound's stability under various conditions ensures reliable performance in laboratory settings, making it a preferred option for researchers focused on developing new therapeutic agents.

In addition to its role in peptide synthesis, Boc-L-a-aminobutyric acid 4-nitrophenyl ester is also valuable in the study of enzyme kinetics and drug design. Its ability to act as a substrate for various enzymes allows researchers to explore biochemical pathways and interactions. Furthermore, the compound's favorable solubility characteristics facilitate its use in diverse formulations, enhancing its applicability in both academic and industrial settings. With its robust profile, this compound stands out as an essential tool for professionals in the fields of organic chemistry and biochemistry.

Synonyms
Boc-L-Abu-ONp, Ester 4-nitrophénylique de l'acide boc-L-2-aminobutanoïque
CAS Number
67708-97-8
Purity
≥ 97 % (HPLC)
Molecular Formula
C15H20N2O6
Molecular Weight
324.2
MDL Number
MFCD00237525
PubChem ID
19359994
Melting Point
75-82 °C
Appearance
Poudre blanc cassé
Optical Rotation
[a] D 20 = -56 ± 2º (C=1 dans MeOH)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Boc-L-Abu-ONp, Ester 4-nitrophénylique de l'acide boc-L-2-aminobutanoïque
CAS Number
67708-97-8
Purity
≥ 97 % (HPLC)
Molecular Formula
C15H20N2O6
Molecular Weight
324.2
MDL Number
MFCD00237525
PubChem ID
19359994
Melting Point
75-82 °C
Appearance
Poudre blanc cassé
Optical Rotation
[a] D 20 = -56 ± 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

Boc-L-a-aminobutyric acid 4-nitrophenyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in peptide synthesis, allowing for the selective modification of amino acids without affecting other functional groups, which is crucial for creating complex peptides.
  • Drug Development: It is used in the development of pharmaceutical compounds, particularly in the design of prodrugs that enhance bioavailability and target specific biological pathways.
  • Bioconjugation: The chemical plays a role in bioconjugation techniques, where it helps attach biomolecules to surfaces or other molecules, facilitating the creation of targeted drug delivery systems.
  • Research in Neuroscience: It is applied in studies related to neurotransmitter modulation, providing insights into neurological functions and potential therapeutic targets for neurodegenerative diseases.
  • Analytical Chemistry: This compound is utilized in analytical methods for quantifying amino acids and peptides, aiding researchers in characterizing complex biological samples.

Citations