13894-14-9

Basic information

• Product Name: Benzenesulfenyl chloride, 4-(1,1-dimethylethyl)-
• CAS NO: 13894-14-9
• Molecular Formula: C10H13ClS
• Molecular Weight: 200.732
• Mol File: 13894-14-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzenesulfenyl chloride, 4-(1,1-dimethylethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfenyl chloride, 4-(1,1-dimethylethyl)-(13894-14-9)
• EPA Substance Registry System: Benzenesulfenyl chloride, 4-(1,1-dimethylethyl)-(13894-14-9)

Safety Data

• Hazardous Substances Data: 13894-14-9(Hazardous Substances Data)

Upstream product

• 2396-68-1 4-t-butylbenzenethiol 

Downstream Products

• 57372-05-1 N'-(3,5-Bis-trifluoromethyl-phenyl)-N-(4-tert-butyl-phenylsulfanyl)-N-methyl-formamidine 
• 57371-69-4 N-(4-tert-Butyl-phenylsulfanyl)-N'-(4-chloro-2-methyl-phenyl)-N-methyl-formamidine 
• 57371-86-5 C₂₀H₂₆N₂S 
• 52145-37-6 Methyl-carbamic acid 4-(4-tert-butyl-phenylsulfanyl)-2,5-dimethyl-phenyl ester 
• 85609-03-6 phenyl p-(tert-butyl)phenyl sulfide 
• 50539-70-3 2,3-Dihydro-2,2-dimethyl-7-benzofuranyl (4-tert-butylphenylthio)(methyl)carbamate 
• 66637-49-8 N-Methyl-N-[4-(tert-butyl)phenylsulfenyl]carbamoyl fluoride 
• 62838-84-0 4,4'-Di-t-butyldibenzolsulfenamid 
• 74880-50-5 (1R,4S,5S,6S)-5-(4-tert-Butyl-phenylsulfanyl)-6-chloro-bicyclo[2.2.1]hept-2-ene 
• 74880-30-1 (1S,2S,3R,4R,6R)-3-(4-tert-Butyl-phenylsulfanyl)-1-chloromethyl-tricyclo[2.2.1.0^2,6]heptane 

Relevant articles and documents

Formation of α-chalcogenyl acrylamides through unprecedented chalcogen-mediated metal-free oxyfunctionalization of ynamides with DMSO as an oxidant

A novel chalcogen-mediated oxyfunctionalization mode of ynamides for the synthesis of α-chalcogenyl acrylamides has been developed. Independent of metal catalysts, external oxidants and additives, this mild process afforded a range of structurally diverse

Generation of Oxazolidine-2,4-diones Bearing Sulfur-Substituted Quaternary Carbon Atoms by Oxothiolation/Cyclization of Ynamides

A novel method for metal-free oxothiolation of ynamides to construct oxazolidine-2,4-diones bearing sulfur-substituted quaternary carbon atoms has been developed. It represents a rare C-O bond cleavage of ynamides, as well as a facile and tandem approach for the formation of C-O, C-S, and C-Cl bonds. This redox-neutral protocol can be applied to the synthesis of multisubstituted oxazolidine-2,4-diones with good chemoselectivity and good yields of isolated products under mild conditions.

N-[4-(Tert-butyl)phenylsulfenyl]-N-alkylcarbamoyl fluoride compounds

N-[4-(tert-butyl)phenylsulfenyl]-N-alkylcarbamoyl fluoride compounds are useful as intermediates in the preparation of pesticidally active carbamoyloxime compounds.