65925-10-2

Basic information

• Product Name: (2-Phenyl-3,4-dihydro-4-oxoquinazolin-3-yl)acetic acid
• Synonyms: (2-Phenyl-3,4-dihydro-4-oxoquinazolin-3-yl)acetic acid
• CAS NO: 65925-10-2
• Molecular Weight: 280.283
• Mol File: 65925-10-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (2-Phenyl-3,4-dihydro-4-oxoquinazolin-3-yl)acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (2-Phenyl-3,4-dihydro-4-oxoquinazolin-3-yl)acetic acid(65925-10-2)
• EPA Substance Registry System: (2-Phenyl-3,4-dihydro-4-oxoquinazolin-3-yl)acetic acid(65925-10-2)

Safety Data

• Hazardous Substances Data: 65925-10-2(Hazardous Substances Data)

Upstream product

• 118-92-3 anthranilic acid 
• 98-88-4 benzoyl chloride 
• 1022-46-4 2-phenyl-4H-3,1-benzoxazin-4-one 
• 56-40-6 glycine 

Downstream Products

• 72875-67-3 3-benzothiazol-2-ylmethyl-2-phenyl-3H-quinazolin-4-one 
• 70540-58-8 (2-Phenyl-3,4-dihydro-4-oxoquinazolin-3-yl)acetyl chloride 
• 122896-60-0 {platinum(II)(2-phenylquinazoline-(3H)-4-one-3-CH₂COO)2} 
• 122912-26-9 {Ru(2-phenyl-3-(carboxymethyl) quinazoline-(3H)-4-one)2(DMSO)2} 
• 122896-60-0 Pt(C₈H₄N₂O(C₆H₅)(CH₂CO₂))2 
• 340155-57-9 [Fe(C₆H₄CONC(C₆H₅)NCH₂COO)2(H₂O)2] 
• 72737-93-0 (4-oxo-2-phenyl-4H-quinazolin-3-yl)-acetic acid ethyl ester 
• 72737-95-2 (4-oxo-2-phenyl-4H-quinazolin-3-yl)-acetic acidhydrazide 

Relevant articles and documents

Synthesis and study of modified polyvinyl alcohol containing amino acid moieties as anticancer agent

A series of new phthalimides compounds[3-7]a-i were synthesized from reaction of Malic anhydride, phthalic anhydride, nitro phthalic anhydride, 2-phenyl-4H-benzo[d][1,3]oxazin-4-one, 2-(4-nitrophenyl)-4H-benzo[d][1,3]oxazin-4-one with different amino acids as glycine, alanine, valine, leucine, isoleucine, serine, threonine, tyrosine and Phenyl alanine [1]a-i under fusion conditions. Compounds [3-7]a-i react with SOCl2 in the presence of benzene to produce compounds [8-12]a-i. Chemical modification of Poly(vinyl alcohol)were obtained by reaction of PVA with compounds [8-12]a-i using the dimethyl formamide to give compounds [13-17]a-i. The structure of the synthesized compounds was characterized by their analytical and spectral data as, IR spectra, 1H, 13C-NMR, Elemental analysis (CHN), UV-Vis Spectroscopy, Scanning electron microscopy (SEM), Antibacterial activity were screened via two kinds of bacteria. Also, anticancer activity were examined for most of the modified polyvinyl alcohol.

Quinazoline 4-thione or quinazoline-4-one carboxylic acids derivatives

-