14032-03-2

Basic information

• Product Name: Benzene, [(2-chlorocyclohexyl)thio]-
• CAS NO: 14032-03-2
• Molecular Formula: C12H15ClS
• Molecular Weight: 226.77
• Mol File: 14032-03-2.mol
• Article Data: 20

Chemical Properties

• CAS DataBase Reference: Benzene, [(2-chlorocyclohexyl)thio]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [(2-chlorocyclohexyl)thio]-(14032-03-2)
• EPA Substance Registry System: Benzene, [(2-chlorocyclohexyl)thio]-(14032-03-2)

Safety Data

• Hazardous Substances Data: 14032-03-2(Hazardous Substances Data)

Upstream product

• 54815-45-1 ethyl benzenesulfenate 
• 110-83-8 cyclohexene 
• 75-05-8 acetonitrile 
• 931-59-9 benzenesulfenyl chloride 
• 64-19-7 acetic acid 
• 88738-21-0 trimethylsilane 
• 98-09-9 benzenesulfonyl chloride 
• 14032-04-3 trans-2-phenylthiocyclohexanol 
• 60263-75-4 C₁₆H₁₅ClO₂S₂ 
• 930-66-5 1-chlorocyclohexene 
• 108-98-5 thiophenol 
• 882-33-7 diphenyldisulfane 
• 13557-24-9 1-chloroethyl phenyl sulfide 
• 7205-91-6 phenylthiomethyl chloride 

Downstream Products

• 86769-63-3 2-((1R,2S)-2-Phenylsulfanyl-cyclohexyl)-propionic acid ethyl ester 
• 33995-48-1 trans-2-chlorocyclohexyl phenyl sulfone 
• 33995-48-1 (+/-)-cis-1-benzenesulfonyl-2-chloro-cyclohexane 
• 86769-66-6 methyl 2-cyclohexyl-2-methylpropanoate 
• 54683-86-2 2-Cyclohex-1-enyl-2-methyl-propionic acid methyl ester 
• 14352-61-5 methyl cyclohexylacetate 
• 53723-52-7 methyl 1-cyclohexene-1-acetate 
• 61346-65-4 2-cyclohex-1-enyl-propionic acid ethyl ester 
• 219601-33-9 [(2-Benzenesulfinyl-cyclohexyl)-difluoro-methyl]-phosphonic acid diethyl ester 
• 17414-12-9 rac-1-(benzenesulfinyl)cyclohexene 
• 65880-17-3 ethyl 4,5,6,7-tetrahydro-2H-isoindole-1-carboxylate 
• 130519-79-8 2:3,7:8,12:13,17:18-tetrabutanoporphyrin 
• 59059-70-0 1-(phenylsulfonyl)cyclohexene 
• 51649-35-5 4,5,6,7-tetrahydro-2H-isoindole 

Relevant articles and documents

Regioselective Chlorothiolation of Alkenes with Sulfonyl Chlorides

Newly developed sulfonyl chloride-based regioselective chlorothiolation of alkenes has been disclosed; the reaction is compatible with a variety of functional groups and can be scaled up to the gram scale with no loss in yield. The employment of readily a

Lewis acids as co-reagents in sulfenylation reactions

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Highly stereoselective chlorination of β-substituted cyclic alcohols using PPh3-NCS: Factors that control the stereoselectivity

A variety of trans-β-substituted cyclic alcohols were stereoselectively chlorinated to either the corresponding cis-chloride or trans-chloride (inversion or retention of configuration) with good to excellent yields; the stereochemical outcome is determined by the size of the ring and the nature of the β-substituents, especially the electronegativity of the substituted atom. The Royal Society of Chemistry.