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Catalog Number:
02271
CAS Number:
10512-93-3
Z-L-valine 4-nitrophenyl ester
Purity:
≥ 99% (HPLC)
Synonym(s):
Z-L-Val-ONp
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Product Information

Z-L-valine 4-nitrophenyl ester is a valuable compound widely utilized in peptide synthesis and pharmaceutical research. This ester derivative of valine features a 4-nitrophenyl group, enhancing its reactivity and making it an excellent choice for various coupling reactions in the formation of peptides. Its unique structure allows for selective modifications, which is particularly beneficial in the development of bioactive compounds and drug candidates. Researchers appreciate its role in facilitating the synthesis of complex peptides, enabling advancements in therapeutic applications, including cancer treatment and antibiotic development.

The compound's stability and compatibility with various reaction conditions make it a preferred choice among professionals in the pharmaceutical and biochemistry fields. Its ability to serve as a building block in the synthesis of more complex molecules underscores its importance in medicinal chemistry. With its practical applications and potential for innovation, Z-L-valine 4-nitrophenyl ester stands out as a key reagent for researchers aiming to explore new therapeutic avenues.

Synonyms
Z-L-Val-ONp
CAS Number
10512-93-3
Purity
≥ 99% (HPLC)
Molecular Formula
C19H20N2O6
Molecular Weight
372.38
MDL Number
MFCD00038116
PubChem ID
309091
Melting Point
63-70º C
Appearance
Pale yellow powder
Optical Rotation
á20D = -24 ± 2 (c = 2% in DMF)
Conditions
Store at 0-8°C
General Information
Synonyms
Z-L-Val-ONp
CAS Number
10512-93-3
Purity
≥ 99% (HPLC)
Molecular Formula
C19H20N2O6
Molecular Weight
372.38
MDL Number
MFCD00038116
PubChem ID
309091
Melting Point
63-70º C
Appearance
Pale yellow powder
Optical Rotation
á20D = -24 ± 2 (c = 2% in DMF)
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

Z-L-valine 4-nitrophenyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, aiding researchers in developing new therapeutic agents.
  • Drug Development: It plays a crucial role in the pharmaceutical industry for creating prodrugs, enhancing the bioavailability of active pharmaceutical ingredients.
  • Bioconjugation: The ester functionality allows for efficient conjugation with biomolecules, facilitating the development of targeted drug delivery systems.
  • Analytical Chemistry: Used as a standard in chromatography, it helps in the quantification of amino acids and related compounds in various samples.
  • Research in Enzyme Activity: This compound is employed in studies to evaluate the activity of enzymes that hydrolyze ester bonds, providing insights into enzymatic mechanisms.

Citations