120449-42-5

Basic information

• Product Name: Se-phenyl 4-methylbenzenecarboselenothioate
• Synonyms: Se-phenyl 4-methylbenzenecarboselenothioate
• CAS NO: 120449-42-5
• Molecular Weight: 291.275
• Mol File: 120449-42-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Se-phenyl 4-methylbenzenecarboselenothioate(CAS DataBase Reference)
• NIST Chemistry Reference: Se-phenyl 4-methylbenzenecarboselenothioate(120449-42-5)
• EPA Substance Registry System: Se-phenyl 4-methylbenzenecarboselenothioate(120449-42-5)

Safety Data

• Hazardous Substances Data: 120449-42-5(Hazardous Substances Data)

Upstream product

• 33861-17-5 phenyl trimethylsilyl selenide 
• 3335-25-9 4-methylthiobenzoyl chloride 
• 60410-77-7 bis(4-methylbenzenethiocarbonyl) sulphide 
• 23974-72-3 sodium phenylselenide 

Downstream Products

• 3481-62-7 1-<4-(methyl)thiobenzoyl>piperidine 
• 1666-13-3 diphenyl diselenide 
• 102197-60-4 phenylseleno 4-methyl(thiobenzoyl) sulfide 
• 15088-74-1 4-methylbenzoic dithioperoxyanhydride 
• 3335-25-9 4-methylthiobenzoyl chloride 
• 52322-79-9 O-phenyl 4-methylbenzenecarbothioate 
• 26028-04-6 O-ethyl 4-methylbenzenecarbothioate 
• 5977-80-0 O-methyl 4-methylbenzenecarbothioate 
• 16112-33-7 2,5-bis(4-methylphenyl)-1,3,4-thiadiazole 
• 42967-76-0 piperidinium 4-methylbenzenecarbodithiolate 
• 54254-92-1 diethylammonium 4-methylbenzenecarbodithioate 
• 53724-38-2 cyclohexylammonium 4-methylbenzenecarbodithioate 
• 20199-06-8 4-methylthiobenzanilide 
• 64310-34-5 3,4-dihydro-2H-1,3,4-triazole-2-thione 

Relevant articles and documents

Se-Aryl Alkane- or Arenecarboselenothioates: Synthesis and Some Reactions

A series of Se-aryl carboselenothioates 3 (RCSSeAr, R=alkyl, aryl) were synthesized and characterized from the reaction of bis(thioacyl) sulfides 1 with sodium areneselenolates.The thionselenolesters 3 are stable (liquid or crystals) both thermally and to moisture.Reactions of 3 with aliphatic primary and secondary amines gave the corresponding ammonium carbodithioates 8 together with diphenyl diselenide 7.In contrast, treatment with aromatic amines or sodium alcoholates afforded the corresponding thioamides or O-alkyl or O-aryl thionoesters in good yields.The oxidation of 3 with m-chloroperbenzoic acid gave the corresponding sulfides 12 and acyl arylseleno sulfides 13 which are formed by a rearrangement of the ArSe group to the thiocarbonyl sulfur atom.