25460-87-1

Basic information

• Product Name: AC-GLU-NH2
• Synonyms: AC-L-ISOGLUTAMINE;AC-ISOGLN-OH;ACETYL-L-GLUTAMIC ACID ALPHA-AMIDE;AC-GLU-NH2;AC-GLUTAMIC ACID-NH2;N-ALPHA-ACETYL-L-ISOGLUTAMINE;N-ALPHA-ACETYL-L-GLUTAMIC ACID ALPHA-AMIDE;(S)-4-(Acetylamino)-5-amino-5-oxopentanoic acid
• CAS NO: 25460-87-1
• Molecular Formula: C₇H₁₂N₂O₄
• Molecular Weight: 188.18
• Mol File: 25460-87-1.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 582.76 °C at 760 mmHg
• Flash Point: 306.242 °C
• Appearance: /
• Density: 1.291 g/cm³
• Storage Temp.: -15°C
• CAS DataBase Reference: AC-GLU-NH2(CAS DataBase Reference)
• NIST Chemistry Reference: AC-GLU-NH2(25460-87-1)
• EPA Substance Registry System: AC-GLU-NH2(25460-87-1)

Safety Data

• Hazardous Substances Data: 25460-87-1(Hazardous Substances Data)

Usage

Uses

N-Acetyl-L-isoglutamine is the N-Acetyl analogue of L-isoglutamine, an isomer of the non-essential amino acid L-glutamine.

Relevant articles and documents

Two-Step Synthesis of α-Aryl-α-diazoamides as Modular Bioreversible Labels

α-Aryl-α-diazoamides were synthesized in two steps under mild conditions. This expeditious route employs Pd-catalyzed C-H arylation of N-succinimidyl 2-diazoacetate to obtain N-succinimidyl 2-aryl-2-diazoacetates, followed by aminolysis. The ensuing diazo compounds can esterify carboxyl groups in aqueous solution, and the ester products are substrates for an esterase. The broad scope of the synthetic route enables the continued development of diazo compounds in chemical biology.