74282-78-3

Basic information

• Product Name: 3,5-dichlorobenzenesulfenyl chloride
• Synonyms: 3,5-dichlorobenzenesulfenyl chloride
• CAS NO: 74282-78-3
• Molecular Weight: 213.515
• Mol File: 74282-78-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3,5-dichlorobenzenesulfenyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-dichlorobenzenesulfenyl chloride(74282-78-3)
• EPA Substance Registry System: 3,5-dichlorobenzenesulfenyl chloride(74282-78-3)

Safety Data

• Hazardous Substances Data: 74282-78-3(Hazardous Substances Data)

Upstream product

• 99847-98-0 (3,5-dichloro-phenyl)-isopropyl sulfide 
• 137897-99-5 1,2-bis(3,5-dichlorophenyl)disulfane 

Downstream Products

• 128529-41-9 N-<(3,5-dicblorophenyl)thio>-2,4,6-triphenylaniline 
• 133872-26-1 N¹,N⁵-bis<(3,5-dichlorophenyl)thio>-2,4-diphenyl-1,3,5-triazapenta-1,3-diene 
• 90584-50-2 N,N-bis<(3,5-dichlorphenyl)thio>-tert-butylamine 
• 95674-86-5 N,N'-bis<(3,5-dichlorophenyl)thio>benzenecarboximidamide 
• 74282-65-8 N-(3,5-Di-tert-butylphenyl)-3,5-dichlorobenzenesulfenamide 
• 95674-91-2 N,N'-bis<(3,5-dichlorophenyl)thio>-4-chlorobenzenecarboximidamide 
• 178110-38-8 N-(5'-tert-Butyl-4,4''-dichloro-[1,1';3',1'']terphenyl-2'-yl)-S-(3,5-dichloro-phenyl)-thiohydroxylamine 
• 203051-50-7 2'-(3,5-Dichloro-phenylsulfanylamino)-[1,1';3',1'']terphenyl-5'-carbonitrile 
• 1025897-59-9 2'-(3,5-Dichloro-phenylsulfanylamino)-[1,1';3',1'']terphenyl-5'-carboxylic acid ethyl ester 
• 1026495-65-7 4,4''-Dichloro-2'-(3,5-dichloro-phenylsulfanylamino)-[1,1';3',1'']terphenyl-5'-carboxylic acid ethyl ester 
• 619298-03-2 N-[(3,5-dichlorophenyl)thio]-4-formyl-2,6-diphenylaniline 
• 128529-45-3 N-<(3,5-dichlorophenyl)thio>-2,4,6-triphenylanilino radical 
• 86602-19-9 C₁₉H₁₁Cl₄N₂S₂ 
• 133872-37-4 C₂₆H₁₆Cl₄N₃S₂ 

Relevant articles and documents

In Situ Formation of RSCl/ArSeCl and Their Application to the Synthesis of 4-Chalcogenylisocumarins/Pyrones from o-(1-Alkynyl)benzoates and (Z)-2-Alken-4-ynoates

The reaction of diorganyl disulfides or diselenides with PhICl2 in acetonitrile was found for the first time to lead to the in situ formation of organosulfenyl chloride or selenenyl chloride, which enables the regioselective intramolecular chalcogenylacyloxylation of alkynes resulting in the formation of 4-chalcogenylisocumarins/pyrones in good to excellent yields under metal-free conditions.

Process for producing imidazole derivatives

PCT No. PCT/JP97/04708 Sec. 371 Date Jun. 10, 1999 Sec. 102(e) Date Jun. 10, 1999 PCT Filed Dec. 19, 1997 PCT Pub. No. WO98/29395 PCT Pub. Date Jul. 9, 1998The present invention provides a process for producing a compound of the formula (III): wherein R1 and R3 are independently hydrogen or an organic group; R2 is an organic group; and R4 is an optionally substituted aryl. by reacting the compound of formula (I): wherein R1, R2, and R3 are as defined above, with the compound of formula (II):R4-S-Hal(II)wherein R4 is as defined above and Hal is halogen, in the presence of base.