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Catalog Number:
02165
CAS Number:
59486-73-6
Z-D-glutamic acid γ-benzyl ester
Purity:
≥ 99% (HPLC)
Synonym(s):
Z-D-Glu(OBzl)-OH, Z-D-glutamic acid 5-benzyl ester
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Product Information

Z-D-glutamic acid g-benzyl ester is a valuable compound in the realm of organic synthesis and pharmaceutical research. This compound, also known as benzyl (2R)-5-oxo-5-phenylmethoxy-2-(phenylmethoxycarbonylamino)pentanoate, serves as an important building block for the synthesis of various peptides and amino acid derivatives. Its unique structure allows for the introduction of functional groups that can enhance the biological activity of the resulting compounds, making it particularly useful in drug development and medicinal chemistry.

Researchers appreciate Z-D-glutamic acid g-benzyl ester for its versatility in creating complex molecules, which can lead to the discovery of new therapeutic agents. Its application extends to the development of neuroprotective drugs and other pharmaceuticals targeting neurological disorders. The compound's stability and ease of manipulation in synthetic pathways make it a preferred choice for professionals looking to innovate in peptide synthesis and related fields.

Synonyms
Z-D-Glu(OBzl)-OH, Z-D-glutamic acid 5-benzyl ester
CAS Number
59486-73-6
Purity
≥ 99% (HPLC)
Molecular Formula
C20H21NO6
Molecular Weight
371.4
MDL Number
MFCD00077014
PubChem ID
297875
Appearance
White solid
Optical Rotation
[a]20D = 7 - 11 ° (C=2.5 in Ethanol)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Z-D-Glu(OBzl)-OH, Z-D-glutamic acid 5-benzyl ester
CAS Number
59486-73-6
Purity
≥ 99% (HPLC)
Molecular Formula
C20H21NO6
Molecular Weight
371.4
MDL Number
MFCD00077014
PubChem ID
297875
Appearance
White solid
Optical Rotation
[a]20D = 7 - 11 ° (C=2.5 in Ethanol)
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-D-glutamic acid g-benzyl ester 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 development of pharmaceuticals. Its unique structure allows for the introduction of specific functionalities that enhance the therapeutic potential of peptide drugs.
  • Drug Development: Researchers leverage this ester in the design of novel drug candidates, especially in the treatment of neurological disorders. Its ability to cross the blood-brain barrier makes it a valuable candidate for central nervous system-targeted therapies.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps to attach biomolecules to drugs or imaging agents, improving their efficacy and specificity in targeting diseased tissues.
  • Research in Neurochemistry: It plays a role in studying glutamate receptors and neurotransmission, contributing to a better understanding of synaptic functions and potential treatments for neurodegenerative diseases.
  • Analytical Chemistry: This compound is utilized in analytical methods for the detection and quantification of amino acids in biological samples, aiding researchers in metabolic studies and nutritional assessments.

Citations