1058163-35-1

Basic information

• Product Name: 4-(2-hydroxyphenyl)-2-(thiophen-2-yl)-2,3-dihydro-1H-benzo[b][1,4]diazepine
• Synonyms: 4-(2-hydroxyphenyl)-2-(thiophen-2-yl)-2,3-dihydro-1H-benzo[b][1,4]diazepine
• CAS NO: 1058163-35-1
• Molecular Weight: 320.415
• Mol File: 1058163-35-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-(2-hydroxyphenyl)-2-(thiophen-2-yl)-2,3-dihydro-1H-benzo[b][1,4]diazepine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2-hydroxyphenyl)-2-(thiophen-2-yl)-2,3-dihydro-1H-benzo[b][1,4]diazepine(1058163-35-1)
• EPA Substance Registry System: 4-(2-hydroxyphenyl)-2-(thiophen-2-yl)-2,3-dihydro-1H-benzo[b][1,4]diazepine(1058163-35-1)

Safety Data

• Hazardous Substances Data: 1058163-35-1(Hazardous Substances Data)

Upstream product

• 18234-50-9 3-(2-hydroxyphenyl)-1-(thiophen-2-yl)prop-2-en-1-one 
• 95-54-5 1,2-diamino-benzene 
• 88-15-3 2-Acetylthiophene 
• 90-02-8 salicylaldehyde 
• 2875-22-1 (E) -1-(2-hydroxyphenyl)-3-(thiophen-2-yl)prop-2-en-3-one 

Relevant articles and documents

Synthesis, characterization, and antioxidant activity of some new benzodiazepine derivatives

A series of novel 4-(substituted phenyl)-2-(2-thienyl)-2,3-dihydro-1H-benzo[b] [1,4] diazepines (MB1-MB8) has been synthesized from 3-(substituted phenyl)-1-(2-thienyl)prop-2-en-1ones (MC1-MC8). The latter compo

Ga(OTf)3-promoted condensation reactions for 1,5-benzodiazepines and 1,5-benzothiazepines

Condensation reactions of o-phenylenediamine and two equivalents of acetophenone under gallium(III) triflate catalysis produce biaryl-substituted 1,5-benzodiazepines. Similar reactions of o-phenylenediamine or o-aminothiophenol and o-hydroxy chalcones lead to formation of functionalized 1,5-benzodiazepines and 1,5-benzothiazepines in good to excellent yields. The ortho-hydoxy group of chalcones is crucial for this unprecedented condensation process.