5977-82-2

Basic information

• Product Name: N-({5-[(4-fluorobenzyl)sulfanyl]-4-(4-methylphenyl)-4H-1,2,4-triazol-3-yl}methyl)cyclobutanecarboxamide
• Synonyms: selenobenzamide;Benzenecarboselenoamide
• CAS NO: 5977-82-2
• Molecular Formula: C₇H₇NSe
• Molecular Weight: 410.5076
• Mol File: 5977-82-2.mol
• Article Data: 20

Chemical Properties

• Density: 1.31g/cm³
• Refractive Index: 1.662
• CAS DataBase Reference: N-({5-[(4-fluorobenzyl)sulfanyl]-4-(4-methylphenyl)-4H-1,2,4-triazol-3-yl}methyl)cyclobutanecarboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-({5-[(4-fluorobenzyl)sulfanyl]-4-(4-methylphenyl)-4H-1,2,4-triazol-3-yl}methyl)cyclobutanecarboxamide(5977-82-2)
• EPA Substance Registry System: N-({5-[(4-fluorobenzyl)sulfanyl]-4-(4-methylphenyl)-4H-1,2,4-triazol-3-yl}methyl)cyclobutanecarboxamide(5977-82-2)

Safety Data

• Hazardous Substances Data: 5977-82-2(Hazardous Substances Data)

Upstream product

• 100-47-0 benzonitrile 
• 55-21-0 benzamide 
• 64-17-5 ethanol 
• 7664-41-7 ammonia 

Downstream Products

• 182572-47-0 N-[1-Dimethylamino-eth-(E)-ylidene]-selenobenzamide 
• 161126-79-0 4-Dimethylamino-4-methyl-2-phenyl-1-selena-3-azabuta-1,3-diene 
• 65599-20-4 3,5-diphenyl-1,2,4-selenadiazole 
• 138278-82-7 4-(4-chlorophenyl)-2-phenyl-1,3-selenazole 
• 100-47-0 benzonitrile 
• 135249-85-3 bis(3-chlorobenzoyl) selenide 
• 38572-14-4 bis(benzoyl) selenide 
• 65212-13-7 bis(4-methylbenzoic) selenoanhydride 
• 65212-14-8 bis(4-chlorobenzoyl) selenide 
• 65212-15-9 bis(4-methoxybenzoic) selenoanhydride 

Relevant articles and documents

Palladium-catalyzed formation of 3,5-diaryl-1,2,4-selenadiazoles from arylselenocarboxamide

A number of new and known arylselenocarboxamides (i.e. Ar-C(=Se)NH2; Ar=C6H5 (1), 4-BrC6H4 (2), 2-MeOC6H4 (3), 4-MeOC6H4 (4), 4-MeSC6H4/sub

A synthetic and structural study of arylselenoamides and 2,4-diaryl-1,3- selenazoles

The systematic preparation of 2,4-diaryl-1,3-selenazoles was carried out by two-component cyclization of the primary selenoamides with α-halo ketones. Selenoamides were obtained from the reaction of Woollins' reagent with arylnitrile, followed by hydrolys

Synthesis and antitumor-evaluation of 1,3-selenazole-containing 1,3,4-thiadiazole derivatives

A series of novel 1,3-selenazole-containing 1,3,4-thiadiazole derivatives bearing Schiff base moieties were synthesized and evaluated for their in vitro antiproliferative activities against human breast cancer cell MCF-7 and mouse lymphocyte leukemia cell