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Catalog Number:
05533
CAS Number:
16947-07-2
Boc-L-glutamic acid े-methyl ester ॅ-4-nitrophenyl ester
Purity:
≥ 99% (TLC)
Synonym(s):
Boc-L-Glu(OMe)-ONp
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Product Information

Boc-L-glutamic acid g-methyl ester a-4-nitrophenyl ester is a versatile compound widely utilized in peptide synthesis and medicinal chemistry. This compound features a protective Boc (tert-butyloxycarbonyl) group, which is essential for the selective modification of amino acids, making it invaluable in the development of complex peptides and pharmaceuticals. Its unique structure allows for the introduction of a nitrophenyl group, enhancing its reactivity and enabling the formation of various derivatives that can be tailored for specific applications in drug development and biochemical research.

Researchers and industry professionals appreciate this compound for its ability to facilitate the synthesis of bioactive peptides, which are crucial in therapeutic applications, including cancer treatment and hormone regulation. The g-methyl ester functionality further enhances its solubility and stability, making it easier to handle in laboratory settings. With its combination of protective groups and reactive sites, Boc-L-glutamic acid g-methyl ester a-4-nitrophenyl ester stands out as a key building block in the synthesis of novel compounds, offering significant advantages over similar products in terms of efficiency and versatility.

Synonyms
Boc-L-Glu(OMe)-ONp
CAS Number
16947-07-2
Purity
≥ 99% (TLC)
Molecular Formula
C17H22N2O8
Molecular Weight
382.36
MDL Number
MFCD00190793
PubChem ID
78438602
Melting Point
86-91 °C
Appearance
White powder with a hint of yellow
Optical Rotation
[a]D24 = -36 ± 2º (C=1% in acetone)
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-L-Glu(OMe)-ONp
CAS Number
16947-07-2
Purity
≥ 99% (TLC)
Molecular Formula
C17H22N2O8
Molecular Weight
382.36
MDL Number
MFCD00190793
PubChem ID
78438602
Melting Point
86-91 °C
Appearance
White powder with a hint of yellow
Optical Rotation
[a]D24 = -36 ± 2º (C=1% in acetone)
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

Boc-L-glutamic acid g-methyl ester a-4-nitrophenyl 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 protective groups allow for selective reactions, enhancing the efficiency of peptide assembly.
  • Drug Development: It is used in the design of drug candidates that target specific biological pathways. The nitrophenyl group can facilitate the study of drug interactions, making it valuable in medicinal chemistry.
  • Bioconjugation: The compound can be employed in bioconjugation processes, linking biomolecules for therapeutic applications. This is particularly useful in creating targeted drug delivery systems.
  • Analytical Chemistry: It finds application in analytical methods for detecting and quantifying amino acids and peptides, aiding researchers in quality control and formulation development.
  • Research in Neurobiology: Due to its structure, it can be used in studies related to neurotransmitter pathways, contributing to the understanding of neurological disorders and potential treatments.

Citations