193539-80-9

Basic information

• Product Name: 2H-1,5-Benzodiazepine-2-thione, 1,3-dihydro-7-(4-methoxyphenoxy)-4-(4-methylphenyl)-
• CAS NO: 193539-80-9
• Molecular Formula: C23H20N2O2S
• Molecular Weight: 388.49
• Mol File: 193539-80-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2H-1,5-Benzodiazepine-2-thione, 1,3-dihydro-7-(4-methoxyphenoxy)-4-(4-methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-1,5-Benzodiazepine-2-thione, 1,3-dihydro-7-(4-methoxyphenoxy)-4-(4-methylphenyl)-(193539-80-9)
• EPA Substance Registry System: 2H-1,5-Benzodiazepine-2-thione, 1,3-dihydro-7-(4-methoxyphenoxy)-4-(4-methylphenyl)-(193539-80-9)

Safety Data

• Hazardous Substances Data: 193539-80-9(Hazardous Substances Data)

Upstream product

• 43156-26-9 4-(p-methoxyphenoxy)-1,2-phenylendiamine 
• 50850-01-6 3,3-dimercapto-1-(p-methylphenyl)-2-propen-1-one 

Downstream Products

• 231956-18-6 7-(p-methoxyphenoxy)-4-(p-methylphenyl)-2-methylthio-3H-[1,5]benzodiazepine 

Relevant articles and documents

Synthesis and spectral properties of 2-methylthio-3H-7-[(o-; m- and p-substituted)phenoxy]-4-(p-substituted-phenyl)-[1,5]benzodiazepines

A series of eleven new 2-methylthio-3H-7-[(o-; m- and p-substituted) phenoxy]-4-(p-substituted-phenyl)-[1,5]benzodiazepines, which have potentially useful pharmacological activities, has been synthesized by condensing the 4-[(o-; m- and p-R1)phenoxy]-1,2-phenylendiamines with 3,3-dimercapto-l-(p-R2-phenyl)-2-propen-1-one. Afterward the 1H-[1,5]benzodiazepine-2-thiones obtained were treated with sodium hydride and methyl iodide. The structure of all products was corroborated by ir, 1H nmr, 13C nmr and ms.

Synthesis and spectral properties of 2,3-dihydro-4-(paramethylphenyl)- 7-[(o-, m-, and p-substituted)phenoxy]-1H-1,5-benzodiazepine-2-thiones

A series of twelve new 2,3-dihydro-4-(para-methylphenyl)-7-[(o-, m-, and p-substituted)phenoxy]-1H-1,5-benzodiazepine-2-thiones, which have potentially useful pharmacological properties, has been synthesized by condensing the 3,3-dimercapto-1-(p-methylphenyl)-2-propen-1-one with 3,4- diaminophenyl-R-phenyl ethers. The structure of all products was corroborated by ir; 1H-nmr; 13C-nmr and ms.