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CHLOROMETHYL PHENYL SULFIDE

CAS No.
7205-91-6
Chemical Name:
CHLOROMETHYL PHENYL SULFIDE
Synonyms
(phenylthio)methyl chloride;Chlorothioanisole;α-Chlorothioanisole;ALPHA-CHLOROTHIOANISOLE;α-Chlorothioanisole >[(chloromethyl)thio]benzene;CHLOROMETHYL PHENYL SULFIDE;chloromethylsulfanylbenzene;chloromethylephenyl sulfide;CHLOROMETHYL PHENYL SULPHIDE
CBNumber:
CB5755381
Molecular Formula:
C7H7ClS
Molecular Weight:
158.65
MDL Number:
MFCD00000921
MOL File:
7205-91-6.mol
MSDS File:
SDS
Last updated:2023-06-08 17:06:38

CHLOROMETHYL PHENYL SULFIDE Properties

Boiling point 66 °C/0.2 mmHg (lit.)
Density 1.184 g/mL at 25 °C (lit.)
refractive index n20/D 1.594(lit.)
Flash point 214 °F
storage temp. 2-8°C
form Liquid
color Clear colorless to pale yellow
Sensitive Stench
BRN 1617369
InChIKey LLSMWLJPWFSMCP-UHFFFAOYSA-N
CAS DataBase Reference 7205-91-6(CAS DataBase Reference)
FDA UNII SF6BSS54L2

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
Safety Statements  23-24/25
RIDADR  UN 3334
WGK Germany  3
10-13
Hazard Note  Stench
HazardClass  4.1
PackingGroup  III
HS Code  29309099
NFPA 704
1
0 0

CHLOROMETHYL PHENYL SULFIDE price More Price(11)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 216631 Chloromethyl phenyl sulfide 97% 7205-91-6 5g $58.56 2024-03-01 Buy
Sigma-Aldrich 216631 Chloromethyl phenyl sulfide 97% 7205-91-6 25g $158.4 2024-03-01 Buy
TCI Chemical C0912 α-Chlorothioanisole >95.0%(GC) 7205-91-6 5g $54 2024-03-01 Buy
TCI Chemical C0912 α-Chlorothioanisole >95.0%(GC) 7205-91-6 25g $158 2024-03-01 Buy
TRC C382070 Chloromethyl phenyl sulfide 7205-91-6 50mg $45 2021-12-16 Buy
Product number Packaging Price Buy
216631 5g $58.56 Buy
216631 25g $158.4 Buy
C0912 5g $54 Buy
C0912 25g $158 Buy
C382070 50mg $45 Buy

CHLOROMETHYL PHENYL SULFIDE Chemical Properties,Uses,Production

Uses

Reagent for the high-yield thiomethylation of O-silylated lactone and ester enolates in the synthesis of α-methylene lactones and esters.1

Uses

Reagent for the high-yield thiomethylation of O-silylated lactone and ester enolates in the synthesis of α-methylene lactones and esters.

Purification Methods

Dissolve the sulfide in CH2Cl2 or CCl4 and dry it (CaCl2), or pass it through a tube of CaCl2 and distil it using a fractionating column. Harmful vapours. It gives the sulfone [7205-98-3] (b 130o/1mm and m 53o from EtOH) [Beilstein 6 IV 1507] on oxidation with permonophthalic acid. [B.hme et al. Justus Liebigs Ann Chem 563 54 64 1949.] [Beilstein 6 III 1002.]

CHLOROMETHYL PHENYL SULFIDE Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 123)Suppliers
Supplier Tel Email Country ProdList Advantage
Capot Chemical Co.,Ltd.
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Dayang Chem (Hangzhou) Co.,Ltd.
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CD Chemical Group Limited
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+8617732866630 bess@weibangbio.com China 18153 58

View Lastest Price from CHLOROMETHYL PHENYL SULFIDE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
CHLOROMETHYL PHENYL SULFIDE pictures 2021-07-02 CHLOROMETHYL PHENYL SULFIDE
7205-91-6
US $15.00-10.00 / KG 1KG 99%+ HPLC Monthly supply of 1 ton Zhuozhou Wenxi import and Export Co., Ltd
CHLOROMETHYL PHENYL SULFIDE pictures 2019-07-11 CHLOROMETHYL PHENYL SULFIDE
7205-91-6
US $3.00 / KG 1KG 99 100kg Career Henan Chemical Co
CHLOROMETHYL PHENYL SULFIDE CHLOROMETHYL PHENYL SULPHIDE ALPHA-CHLOROTHIOANISOLE Chlorothioanisole [(chloromethyl)thio]benzene ALPHA-CHLOROTHIOANISOLE 95+% Benzene, (chloromethyl)thio- Chloromethyl phenyl sulphide 98% CHLOROMETHYL PHENYL SULLFIDE, 97% (chloromethyl)(phenyl)sulfane Phenyl(chloromethyl) sulfide chloromethylsulfanylbenzene [(Chloromethyl)sulphanyl]benzene, alpha-Chlorothioanisole Chloromethyl phenyl sulfide 97% chloromethylephenyl sulfide α-Chlorothioanisole > α-Chlorothioanisole (phenylthio)methyl chloride 7205-91-6 C6H5SCH2Cl Building Blocks Sulfides/Disulfides Sulfur Compounds Organic Building Blocks Building Blocks Chemical Synthesis Organic Building Blocks Sulfides/Disulfides Sulfur Compounds