7205-65-4

Basic information

• Product Name: Benzene, 1-chloro-4-[(1,1-dimethylethyl)thio]-
• CAS NO: 7205-65-4
• Molecular Formula: C10H13ClS
• Molecular Weight: 200.732
• Mol File: 7205-65-4.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Benzene, 1-chloro-4-[(1,1-dimethylethyl)thio]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-chloro-4-[(1,1-dimethylethyl)thio]-(7205-65-4)
• EPA Substance Registry System: Benzene, 1-chloro-4-[(1,1-dimethylethyl)thio]-(7205-65-4)

Safety Data

• Hazardous Substances Data: 7205-65-4(Hazardous Substances Data)

Upstream product

• 106-46-7 para-dichlorobenzene 
• 75-66-1 2-methylpropan-2-thiol 
• 507-19-7 t-butyl bromide 
• 106-54-7 p-Chlorothiophenol 
• 1142-19-4 4,4'-dichlorodiphenyl disulfide 
• 119072-55-8 tert-butylisonitrile 
• 536-74-3 phenylacetylene 
• 163319-00-4 ((C₆H₅)2PCH₂CH₂P(C₆H₅)2)Pd(SC(CH₃)3)(C₆H₄Cl) 
• 24762-44-5 triphenylphosphine-d15 
• 213540-20-6 ((C₆H₅)2PCH₂CH₂P(C₆H₅)2)Pd(SC₆H₄Cl)(C₆H₄C₄H₉) 
• 106-39-8 bromochlorobenzene 
• 75-65-0 tert-butyl alcohol 
• 84379-72-6 1,3-dioxoisoindolin-2-yl 3,3-dimethylbutanoate 
• 691-64-5 di-tert-butyl oxalate 

Downstream Products

• 66724-22-9 6-chloro-2-phenyl-4H-thiochromen-4-one 
• 128671-31-8 (E)-3-(4-Chloro-phenylsulfanyl)-3-phenyl-acrylic acid ethyl ester 
• 128671-25-0 ethyl (Z)-3-((4-chlorophenyl)thio)-3-phenylacrylate 
• 87544-11-4 1-Methanesulfonyl-4-(2-methyl-propane-2-sulfonyl)-benzene 
• 7205-75-6 p-Chlorphenyl-1,1-dimethylaethylsulfoxid 
• 7205-86-9 tert-butyl(4-chlorophenyl)sulfone 
• 87544-10-3 p-(methylthio)phenyl t-butyl sulphide 

Relevant articles and documents

Zn- And Cu-catalyzed coupling of tertiary alkyl bromides and oxalates to forge challenging C?O, C?S, and C?N bonds

We describe here the facile construction of sterically hindered tertiary alkyl ethers and thioethers via the Zn(OTf)2catalyzed coupling of alcohols/phenols with unactivated tertiary alkyl bromides and the Cu(OTf)2-catalyzed thiolation of unactivated tertiary alkyl oxalates with thiols. The present protocol represents one of the most effective unactivated tertiary C(sp3)? heteroatom bond-forming conditions via readily accessible Lewis acid catalysis that is surprisingly less developed.

Visible-Light-Mediated Alkylation of Thiophenols via Electron Donor-Acceptor Complexes Formed between Two Reactants

A metal-free, photocatalyst-free, photochemical system was developed for the direct alkylation of thiophenols via electron donor-acceptor (EDA) complexes (KEDA = 145 M-1) between two reactants, N-hydroxyphthalimide esters as acceptors and thiophenol anions as donors, in the presence of a tertiary amine. The EDA complexes in the reaction system have a broad range of visible-light absorption (400-650 nm) and can trigger the reaction effectively under sunlight.

Oxidation of Organosulfides to Organosulfones with Trifluoromethyl 3-Oxo-1λ 3,2-benziodoxole-1(3 H)-carboxylate as an Oxidant

An alternative approach is described for the oxidation of organosulfides to the corresponding organosulfones by using trifluoromethyl 3-oxo-1λ 3,2-benziodoxole-1(3 H)-carboxylate as an oxidant. The oxidation of the sulfides was performed by using 2.4 equivalents of the oxidant in refluxing acetonitrile. The oxidation products were isolated in good to excellent yields.