42288-24-4

Basic information

• Product Name: Glycine, N-(4-acetylphenyl)-
• CAS NO: 42288-24-4
• Molecular Formula: C10H11NO3
• Molecular Weight: 193.202
• Mol File: 42288-24-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Glycine, N-(4-acetylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Glycine, N-(4-acetylphenyl)-(42288-24-4)
• EPA Substance Registry System: Glycine, N-(4-acetylphenyl)-(42288-24-4)

Safety Data

• Hazardous Substances Data: 42288-24-4(Hazardous Substances Data)

Upstream product

• 100-19-6 (4-nitrophenyl)ethanone 
• 99-92-3 p-aminobenzophenone 
• 79-11-8 chloroacetic acid 
• 127-09-3 sodium acetate 
• 79-08-3 bromoacetic acid 

Downstream Products

• 154136-93-3 [4-((E)-3-Pyridin-2-yl-acryloyl)-phenylamino]-acetic acid 
• 1062017-99-5 2-((4-acetylphenyl)amino)-1-(4-(4-methoxyphenyl)piperazin-1-yl)ethanone 
• 84968-94-5 3-<4-<3-(4-nitrophenyl)-1-oxo-2-propenyl>phenyl>sydnone 
• 84969-02-8 C₁₉H₁₆N₂O₅ 
• 84968-92-3 3-<4-<3-(4-methoxyphenyl)-1-oxo-2-propenyl>-phenyl>sydnone 
• 84968-96-7 C₁₇H₁₂N₂O₄ 
• 84968-93-4 3-<4-<3-(4-chlorophenyl)-1-oxo-2-propenyl>phenyl>sydnone 
• 84969-03-9 3-<4-<3-(4-methylphenyl)-1-oxo-2-propenyl>phenyl>sydnone 
• 84968-91-2 3-<4-<1-oxo-3-phenyl-2-propenyl>phenyl>sydnone 
• 84969-12-0 1-(p-acetylphenyl)pyrazole-3,4-dicarboxylic acid methyl ester 
• 84968-90-1 4-bromo-3-[p-(acetyl)phenyl]sydnone 
• 143391-45-1 3-<4-<3-(4-nitrophenyl)-2,3-dibromopropionyl>phenyl>sydnone 
• 143391-44-0 N-nitroso-N-<4-<3-(4-nitrophenyl)-2,3-dibromopropionyl>phenyl>glycine 
• 143391-39-3 C₁₇H₁₁N₃O₅ 

Relevant articles and documents

Non-natural amino acid and application thereof Recombinant protein and recombinant protein conjugate comprising same

The invention provides a non-natural amino acid. A compound represented by formula (I) or an enantiomer thereof. The invention also provides application of the non-natural amino acid. Further, the present invention also provides a protein conjugate comprising the recombinant protein and of the non-natural amino acid prepared from the recombinant protein. The non-natural amino acid provided by the invention is simple and convenient to prepare, good in safety, not prone to inactivation during protein insertion, high in conjugate rate with a coupling part, and higher in stability of the obtained conjugate.

Synthesis and antimicrobial activity of 3-(substituted-phenyl)-sydnones

3-(3 or 4-Acetylphenyl)-sydnones 7, 8 have been synthesized by formation of the glycines 3, 4, followed by nitrosation to 5, 6 and cyclization with acetic anhydride to sydnones. Sydnone derivatives carrying chalcone moieties 15, 16 were prepared by format