38880-89-6

Usage

InChI:InChI=1/C13H10N2O4/c16-12-8-10(15(18)19)6-7-11(12)14-13(17)9-4-2-1-3-5-9/h1-8,16H,(H,14,17)

Upstream product

• 98-88-4 benzoyl chloride 
• 121-88-0 5-Nitro-2-aminophenol 
• 3393-96-2 p-nitrobenzanilide 

Downstream Products

• 114260-52-5 2-Hydroxy-N-(2-hydroxy-4-nitro-phenyl)-benzamide 
• 137470-78-1 2-(2-Benzoylamino-5-nitro-phenoxy)-N-(2-hydroxy-4-nitro-phenyl)-benzamide 
• 137444-97-4 2-(2-Benzoylamino-5-nitro-phenoxy)-6-hydroxy-N-(2-hydroxy-4-nitro-phenyl)-benzamide 
• 137444-98-5 2-(2-Benzoylamino-5-nitro-phenoxy)-N-(2-benzoylamino-5-nitro-phenyl)-6-hydroxy-N-(2-hydroxy-4-nitro-phenyl)-benzamide 
• 3164-28-1 6-nitro-2-phenylbenzo[d]oxazole 
• 38880-91-0 N-[2-Hydroxy-4-(2-methyl-acryloylamino)-phenyl]-benzamide 
• 112764-65-5 1-benzoyl-7-(benzyloxy)-4-bromo-3-methyl-N⁵-(phenylsulfonyl)-5-(2-propyn-1-ylamino)indole 
• 112764-66-6 6-benzoyl-5-(benzyloxy)-1,2-dihydro-1-(hydroxymethyl)-8-methyl-3-(phenylsulfonyl)-3H-pyrrolo<3,2-e>indole 
• 112793-55-2 6-benzoyl-5-(benzyloxy)-1,2-dihydro-8-methyl-1-methylidene-3-(phenylsulfonyl)-3H-pyrrolo<3,2-e>indole 
• 112764-64-4 5-amino-1-benzoyl-7-(benzyloxy)-4-bromo-3-methyl-N⁵-(phenylsulfonyl)indole 
• 112764-67-7 (1RS)-3-(Benzenesulfonyl)-5-(benzyloxy)-1-(hydroxymethyl)-8-methyl-1,2-dihydro-3H-pyrrolo<3,2-e>indole 
• 175614-07-0 (+/-)-(1R*)-5-(benzyloxy)-3-<(tert-butyloxy)carbonyl>-1-(chloromethyl)-8-methyl-1,2-dihydro-3H-pyrrolo<3,2-e>indole 
• 112089-71-1 (+/-)-(1R*)-5-(benzyloxy)-3-<(tert-butyloxy)carbonyl>-1-(hydroxymethyl)-8-methyl-1,2-dihydro-3H-pyrrolo<3,2-e>indole 
• 112793-56-3 (1RS)-3-Benzenesulfonyl-5-hydroxy-1-hydroxymethyl-8-methyl-1,2-dihydro-3H-pyrrolo[3,2-e]indole 

Relevant academic research and scientific papers

A diversity-oriented synthesis of bioactive benzanilides via a regioselective C(sp2)-H hydroxylation strategy

A diversity-oriented synthesis of bioactive benzanilides via C(sp2)-H hydroxylation has been studied. Different regioselectivity was observed with Ru(ii) and Pd(ii) catalysts. The reaction demonstrates excellent regioselectivity, good tolerance

Synthesis and biological evaluation of new N-(2-hydroxy-4(or 5)-nitro/aminophenyl)benzamides and phenylacetamides as antimicrobial agents

A new series of N-(2-hydroxy-4(or 5)-nitro/aminophenyl)benzamide and phenylacetamide derivatives (1a-1n, 2a-2n) were synthesized and evaluated for antibacterial and antifungal activities against Staphylococcus aureus, Bacillus subtilis, Klebsiella pneumoniae, Pseudomonas aeruginosa, Escherichia coli, Candida albicans, and their drug-resistant isolate. Microbiological results indicated that the compounds possessed a broad spectrum of activity against the tested microorganisms at MIC values between 500 and 1.95 μg/ml. Benzamide derivative 1d exhibited the greatest activity with MIC values of 1.95, 3.9, and 7.8 μg/ml against drug-resistant B. subtilis, B. subtilis, and S. aureus, respectively.