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136344

Sigma-Aldrich

Chloromethyl 4-chlorophenyl sulfide

97%

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About This Item

Linear Formula:
ClC6H4SCH2Cl
CAS Number:
7205-90-5
Molecular Weight:
193.09
EC Number:
230-578-1
MDL number:
MFCD00000922
UNSPSC Code:
12352100
PubChem Substance ID:
24848277

assay

97%

form

liquid

refractive index

n20/D 1.6065 (lit.)

bp

128-129 °C/12 mmHg (lit.)

density

1.348 g/mL at 25 °C (lit.)

functional group

chloro
thioether

storage temp.

2-8°C

SMILES string

ClCSc1ccc(Cl)cc1

InChI

1S/C7H6Cl2S/c8-5-10-7-3-1-6(9)2-4-7/h1-4H,5H2

InChI key

XPJUCMIJGVAEGF-UHFFFAOYSA-N

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Application

Chloromethyl 4-chlorophenyl sulfide was used to study the solvolysis of chloromethyl phenyl sulfide [(phenylthio)methyl chloride] and its p-chloro-derivative in a wide range of hydroxylic solvents[1]. It was used as starting reagent in the synthesis of (4-chlorophenylthio) methyl acetate[2]. It was used as alkylating reagent in microwave-assisted synthesis of 2-amino-imidazo[1,2-a]pyridine derivatives[3].

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

No data available

flash_point_c

No data available

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
36096PK
MKBC2409
MKBB8095
05107TD
03128JB

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A new approach to the synthesis of 2-aminoimidazo [1, 2-a]pyridine derivatives through microwave-assisted N-alkylation of 2-halopyridines.
Vega JA, et al.
Tetrahedron, 55(8), 2317-2326 (1999)
Dennis N Kevill et al.
Current organic chemistry, 16(12), 1502-1511 (2012-06-20)
The specific rates of solvolysis of chloromethyl phenyl sulfide [(phenylthio)methyl chloride] and its p-chloro-derivative have been determined at 0.0 °C in a wide range of hydroxylic solvents, including several containing a fluroalcohol. Treatment in terms of a two-term Grunwald-Winstein equation
Synthesis of α-Haloalkyl Esters from α-Arylthioalkyl Esters.
Benneche T, et al.
Acta Chemica Scandinavica, 43, 74-77 (1988)

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