7205-94-9

Basic information

• Product Name: CHLOROMETHYL PHENYL SULFOXIDE
• Synonyms: CHLOROMETHYL PHENYL SULFOXIDE;[(chloromethyl)sulphinyl]benzene;[(Chloromethyl)sulfinyl]benzene;Phenyl (chloromethyl) sulfoxide;Benzene, ((chloromethyl)sulfinyl)-;Einecs 230-580-2;Chloromethyl phenyl sulfoxide >=97.0%
• CAS NO: 7205-94-9
• Molecular Formula: C₇H₇ClOS
• Molecular Weight: 174.65
• EINECS: 230-580-2
• Product Categories: Organic Building Blocks;Sulfoxides;Sulfur Compounds
• Mol File: 7205-94-9.mol
• Article Data: 30

Chemical Properties

• Melting Point: 33-35 °C
• Boiling Point: 109-111 °C0.01 mm Hg
• Flash Point: 100 °C
• Appearance: /
• Density: 1.35g/cm³
• Vapor Pressure: 0.00125mmHg at 25°C
• Refractive Index: 1.618
• Storage Temp.: −20°C
• BRN: 1617664
• CAS DataBase Reference: CHLOROMETHYL PHENYL SULFOXIDE(CAS DataBase Reference)
• NIST Chemistry Reference: CHLOROMETHYL PHENYL SULFOXIDE(7205-94-9)
• EPA Substance Registry System: CHLOROMETHYL PHENYL SULFOXIDE(7205-94-9)

Safety Data

• Safety Statements: 22-24/25
• WGK Germany: 3
• Hazardous Substances Data: 7205-94-9(Hazardous Substances Data)

Usage

Uses

Chloromethyl phenyl sulfoxide has been used in the preparation of:1-chloroalkyl sulfoxidesstarting material for the synthesis alkyl sulfoxides and thiol ester acyl anion equivalent

Synthesis Reference(s)

Journal of the American Chemical Society, 90, p. 4496, 1968 DOI: 10.1021/ja01018a078Synthesis, p. 831, 1986Tetrahedron Letters, 17, p. 613, 1976

General Description

Chloromethyl phenyl sulfoxide has synthetic potential and exhibits unusual stereochemical specificity. Stereospecific hydroxyalkylation of chloromethyl phenyl sulfoxide has been investigated.

InChI:InChI=1/C7H7ClOS/c8-6-10(9)7-4-2-1-3-5-7/h1-5H,6H2

Upstream product

• 186581-53-3 diazomethane 
• 4972-29-6 benzenesulphinyl chloride 
• 60-29-7 diethyl ether 
• 100-68-5 methyl-phenyl-thioether 
• 7205-91-6 phenylthiomethyl chloride 
• 1193-82-4 racemic methyl phenyl sulfoxide 

Downstream Products

• 21849-27-4 1-(Phenylsulfinylchlormethyl)-cyclohexanol 
• 29626-90-2 1-chloro-2-phenylethyl phenyl sulfoxide 
• 38042-52-3 2-chloro-2-(phenylsulfinyl)-1-phenyl-1-ethanone 
• 121000-76-8 1-[chloro (phenylsulfinyl)methyl]-2-cyclohexene-1-ol 
• 41103-68-8 1-(phenylsulfinyl)undecan-2-one 
• 64190-24-5 1-cyclobutanol 
• 145663-76-9 1-cyclodecanol 
• 128867-19-6 2-Benzenesulfinyl-2-chloro-1-naphthalen-1-yl-ethanol 
• 111036-60-3 2-Benzenesulfinyl-6-tert-butyl-1-oxa-spiro[2.5]octane 
• 18245-74-4 S-phenyl 2-phenylethanethioate 
• 63988-06-7 1-chloro-1-phenylsulfinylhexan-2-ol 
• 192879-36-0 2-chloro-1-cyclohexyl-2-(phenylsulfinyl)-1-ethanone 
• 889877-31-0 2-(phenylsulfinylmethylthio)benzenamine 
• 21849-30-9 2-benzenesulfinyl-1-oxa-spiro[2.5]octane 

Relevant articles and documents

Aldehyde to Ketone Homologation Enabled by Improved Access to Thioalkyl Phosphonium Salts

Phosphines were previously unusable as Pummerer-type nucleophiles due to competing redox chemistry with sulfoxides. Here we circumvent this problem to achieve a formal phosphine Pummerer reaction that offers thioalkyl phosphonium salts that, in turn, give rise to diverse vinyl sulfides via Wittig olefinations. Thirty vinyl sulfides are thus prepared from (alkylthioalkyl)triphenyl phosphonium salts and aldehydes. The hydrolysis of these vinyl sulfides offers an efficient and versatile two-step one-carbon homologation of aldehydes to ketones.

Sulfone compound (by machine translation)

[Problem] to safely and conveniently, highly selective, sulfide compound producing a sulfone compound. [Solution] pH is 9 - 12 under, water or water-insoluble solvent or an aromatic hydrocarbon-based solvent mixture, sodium hypochlorite is used as oxidizing agent, (1) (2) from the compound represented by the formula sulfide sulfone compound represented by the formula manufacturing method. (R1 And R2 Are each independently an alkyl, aryl, aralkyl, heteroaryl)[Drawing] no (by machine translation)

On the nature of the chain-extending species in organolithium initiated stereospecific reagent-controlled homologation reactions using α-chloroalkyl aryl sulfoxides

The reaction of an organolithium with an α-chloroalkyl aryl sulfoxide ostensibly generates an α-chloroalkyllithium by sulfoxide-lithium exchange, but the actual identity of the chain-extending species in chlorosulfoxide-based StReCH reactions is not certain. To explore this issue, racemic 2-cyclohexyl (4R?,5R?)-4,5-diphenyl-1,3,2-dioxaborolane was homologated by treatment with scalemic (S)-chloromethyl phenyl sulfoxide and n-BuLi (THF, -78 °C). The reaction proceeded without a detectable level of kinetic resolution, a finding consistent with chloromethyllithium being the active chain-extending species rather than a chiral sulfurane intermediate.