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Catalog Number:
01346
CAS Number:
15387-45-8
Ester de boc-L-glutamine 4-nitrophényle
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-L-Gln-ONp
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Product Information

Substrat pour la cathepsine B.

Synonyms
Boc-L-Gln-ONp
CAS Number
15387-45-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C16H21N3O7
Molecular Weight
367.4
MDL Number
MFCD00065572
PubChem ID
85834
Melting Point
142-148 °C
Appearance
Poudre blanche
Optical Rotation
[α] D 20 = -33 ± 2º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Boc-L-Gln-ONp
CAS Number
15387-45-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C16H21N3O7
Molecular Weight
367.4
MDL Number
MFCD00065572
PubChem ID
85834
Melting Point
142-148 °C
Appearance
Poudre blanche
Optical Rotation
[α] D 20 = -33 ± 2º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-L-glutamine 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, particularly in solid-phase peptide synthesis, allowing for the efficient coupling of amino acids.
  • Drug Development: It is employed in the development of pharmaceutical compounds, especially those targeting glutamine pathways, which are crucial in cancer metabolism and other diseases.
  • Bioconjugation: The ester functionality enables bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, enhancing drug delivery systems.
  • Analytical Chemistry: Used as a standard in chromatographic techniques, it helps in the quantification and analysis of glutamine derivatives in various samples.
  • Research in Neurobiology: Its role in studying neurotransmitter pathways makes it significant for research into neurological disorders, providing insights into glutamate and its analogs.

Citations