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Catalog Number:
21796
CAS Number:
13726-52-8
N-(4-Aminobenzoyl)-L-glutamic acid diethyl ester
Synonym(s):
Diethyl N-(4-aminobenzoyl)-L-glutamate
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Product Information

N-(4-Aminobenzoyl)-L-glutamic acid diethyl ester is a versatile compound with significant applications in the fields of pharmaceuticals and biochemistry. This diethyl ester derivative of L-glutamic acid features an amino group that enhances its reactivity and potential for use in drug formulation. Its unique structure allows it to serve as an important intermediate in the synthesis of various bioactive molecules, particularly in the development of peptide-based therapeutics. Researchers have utilized this compound in studies related to drug delivery systems and as a building block for more complex molecular architectures, making it invaluable in medicinal chemistry.

The compound's ability to form stable conjugates with other biomolecules opens up avenues for targeted drug delivery, enhancing therapeutic efficacy while minimizing side effects. Its solubility and compatibility with various solvents further support its use in diverse formulations. As a result, N-(4-Aminobenzoyl)-L-glutamic acid diethyl ester stands out for its potential in advancing research and development in drug design and delivery systems, making it a key asset for professionals in the pharmaceutical industry.

Synonyms
Diethyl N-(4-aminobenzoyl)-L-glutamate
CAS Number
13726-52-8
Molecular Formula
C16H22N2O5
Molecular Weight
322.36
MDL Number
MFCD00009617
PubChem ID
256289
Conditions
Store at 0-8°C
General Information
Synonyms
Diethyl N-(4-aminobenzoyl)-L-glutamate
CAS Number
13726-52-8
Molecular Formula
C16H22N2O5
Molecular Weight
322.36
MDL Number
MFCD00009617
PubChem ID
256289
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

N-(4-Aminobenzoyl)-L-glutamic acid diethyl ester is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Bioconjugation: It is used in bioconjugation processes to link biomolecules, enhancing the delivery and efficacy of therapeutic agents in targeted drug delivery systems.
  • Research in Cancer Therapy: The compound plays a role in cancer research, particularly in developing targeted therapies that utilize its properties to inhibit tumor growth.
  • Analytical Chemistry: It is employed as a reagent in analytical methods to detect and quantify amino acids and peptides, providing valuable insights in biochemical research.
  • Food Industry Applications: The compound can be used in food science for the development of flavor enhancers and preservatives, improving food quality and shelf-life.

Citations