73753-35-2

Basic information

• Product Name: 2(3H)-Selenazolone, 4,5-diphenyl-, hydrazone
• CAS NO: 73753-35-2
• Molecular Formula: C15H13N3Se
• Molecular Weight: 314.248
• Mol File: 73753-35-2.mol

Chemical Properties

• CAS DataBase Reference: 2(3H)-Selenazolone, 4,5-diphenyl-, hydrazone(CAS DataBase Reference)
• NIST Chemistry Reference: 2(3H)-Selenazolone, 4,5-diphenyl-, hydrazone(73753-35-2)
• EPA Substance Registry System: 2(3H)-Selenazolone, 4,5-diphenyl-, hydrazone(73753-35-2)

Safety Data

• Hazardous Substances Data: 73753-35-2(Hazardous Substances Data)

Upstream product

• 110152-95-9 propan-2-one (4,5-diphenyl-selenazol-2-yl)-hydrazone 
• 21198-79-8 selenosemicarbazide 
• 1484-50-0 desyl bromide 
• 447-31-4 Desyl chloride 

Downstream Products

• 105432-50-6 2-(4,5-diphenyl-selenazol-2-yl)-5-heptadecyl-1,2-dihydro-pyrazol-3-one 
• 124805-00-1 Bis(4,5-diphenyl-selenazol-2-yl)selenid 
• 124804-99-5 4,4',5,5'-Tetraphenylazoselenazol-(2,2') 
• 7496-79-9 4-phenyl-5-phenylselenazol-2-ylamine 
• 124805-01-2 Acetic acid N'-acetyl-N,N'-bis-(4,5-diphenyl-selenazol-2-yl)-hydrazide 
• 104852-89-3 4-(4-diethylamino-phenylimino)-2-(4,5-diphenyl-selenazol-2-yl)-5-methyl-2,4-dihydro-pyrazol-3-one 
• 103572-53-8 4-(4-dimethylamino-phenylimino)-2-(4,5-diphenyl-selenazol-2-yl)-5-methyl-2,4-dihydro-pyrazol-3-one 

Relevant articles and documents

Synthesis of 1,3-selenazoles and bis(selenazoles) from primary selenocarboxylic amides and selenourea

The reaction of nitriles with P2Se5 in the presence of EtOH-H2O afforded primary selenocarboxylic amides. The cyclization of these compounds with α-halo ketones afforded a variety of functionalized 1,3-selenazoles. The use of P2Se5 also allowed the convenient synthesis of selenocarboxylic diamides which were transformed into bis(selenazol-2-yl)alkanes ('bis-selenazoles'). A practical method for the synthesis of selenourea was developed. This useful small building block was successfully applied to the synthesis of primary 2-amino-1,3- selenazoles.