4834-61-1 (4-苯甲酰基乙酰苯胺,Acetamide,N-(4-benzoylphenyl)-)

4-苯甲酰基乙酰苯胺;

Acetamide,N-(4-benzoylphenyl)-;4-Benzoyl Acetanilide;N-(4-benzoylphenyl)acetamide;4-(ACETYLAMINO)BENZOPHENONE;4-acetamidobenzophenone;4-Acetamodobenzophenone;acetic acid-(4-benzoyl-anilide);Essigsaeure-(4-benzoyl-anilid);N-[4-(phenylcarbonyl)phenyl]acetamide;N-acetyl-4-aminobenzophenone;p-benzoylacetanilide;HMS2285P10;Oprea1_579255;NSC21512;Oprea1_393886;SCHEMBL1851249;4834-61-1;MFCD00566694;OBEXUAPBTUTPDV-UHFFFAOYSA-N;SR-01000199511;HMS1579D05;4-(Benzoyl)acetanilide;AKOS000483899;N-(4-benzoyl-phenyl)-acetamide;4-acetaminobenzophenone;SR-01000199511-1;CHEMBL1389287;NSC-21512;4-BenzoylAcetanilide;MLS000104524;SMR000054459;DTXSID40281396;Cambridge id 5226796;

OBEXUAPBTUTPDV-UHFFFAOYSA-N

1S/C15H13NO2/c1-11(17)16-14-9-7-13(8-10-14)15(18)12-5-3-2-4-6-12/h2-10H,1H3,(H,16,17)

O=C(C1C=CC=CC=1)C1C=CC(=CC=1)NC(C)=O

甲苯咪唑的中间体。;

用对硝基苯甲酸以氯化亚硫酰氯化，生成对硝基苯甲酰氯，然后与苯在无水三氯化铝参与下缩合，生成4-硝基二苯酮，进而还原硝基并以乙酸酐酰化即得该品。