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Catalog Number:
02120
CAS Number:
1168-87-2
Z-L-alanine 4-nitrophenyl ester
Purity:
≥ 99% (HPLC)
Synonym(s):
Z-L-Ala-ONp
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Product Information

Z-L-alanine 4-nitrophenyl ester is a versatile compound widely utilized in the fields of organic synthesis and pharmaceutical research. This ester derivative of Z-L-alanine features a 4-nitrophenyl group, which enhances its reactivity and makes it an excellent candidate for various coupling reactions. Its unique structure allows for the selective modification of amino acids and peptides, facilitating the development of novel therapeutic agents. Researchers often employ Z-L-alanine 4-nitrophenyl ester in the synthesis of peptide-based drugs, where its ability to act as a protecting group is particularly advantageous.

In addition to its applications in drug development, this compound serves as a valuable tool in biochemical studies, enabling scientists to explore enzyme mechanisms and protein interactions. Its stability and ease of handling make it a preferred choice for laboratories focused on peptide synthesis and modification. With its broad range of applications, Z-L-alanine 4-nitrophenyl ester stands out as a crucial reagent for professionals seeking to innovate in the realms of medicinal chemistry and biochemistry.

Synonyms
Z-L-Ala-ONp
CAS Number
1168-87-2
Purity
≥ 99% (HPLC)
Molecular Formula
C17H16N2O6
Molecular Weight
344.3
MDL Number
MFCD00038118
PubChem ID
102569
Melting Point
72 - 76 °C
Appearance
White to off-white powder
Optical Rotation
[a]20D = -52 ± 2 º (C=1 in EtOH)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Z-L-Ala-ONp
CAS Number
1168-87-2
Purity
≥ 99% (HPLC)
Molecular Formula
C17H16N2O6
Molecular Weight
344.3
MDL Number
MFCD00038118
PubChem ID
102569
Melting Point
72 - 76 °C
Appearance
White to off-white powder
Optical Rotation
[a]20D = -52 ± 2 º (C=1 in EtOH)
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-alanine 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, which are essential in drug development and biochemistry.
  • Bioconjugation: It is used in bioconjugation processes to attach biomolecules to surfaces or other molecules, enhancing the functionality of drugs and diagnostics.
  • Fluorescent Probes: The compound can be employed in the development of fluorescent probes for imaging applications, aiding researchers in visualizing cellular processes.
  • Enzyme Inhibition Studies: It is useful in studying enzyme inhibition, providing insights into enzyme mechanisms and potential therapeutic targets.
  • Drug Delivery Systems: This ester can be incorporated into drug delivery systems, improving the solubility and bioavailability of therapeutic agents.

Citations