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C54007

Sigma-Aldrich

Chloromethyl methyl sulfide

95%

Synonym(s):

Chlorodimethyl sulfide

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About This Item

Linear Formula:
CH3SCH2Cl
CAS Number:
2373-51-5
Molecular Weight:
96.58
Beilstein:
1730851
EC Number:
219-148-4
MDL number:
MFCD00000923
UNSPSC Code:
12352101
PubChem Substance ID:
24892780
NACRES:
NA.22

Assay

95%

form

liquid

refractive index

n20/D 1.498 (lit.)

bp

105 °C (lit.)

density

1.153 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

CSCCl

InChI

1S/C2H5ClS/c1-4-2-3/h2H2,1H3

InChI key

JWMLCCRPDOIBAV-UHFFFAOYSA-N

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Application

Methylthiomethylating reagent for carbonyl and aromatic compounds. Methylene transfer reagent for iron(II) mediated cyclopropanation.

Caution

May darken in storage.

Pictograms

Flame
GHS02

Signal Word

Danger

Hazard Statements

H225

Hazard Classifications

Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

62.6 °F - closed cup

Flash Point(C)

17 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Organic Syntheses, 70, 177-177 (1992)
Manuel Algarra et al.
The journal of physical chemistry. A, 124(10), 1911-1921 (2020-02-14)
UV photodecomposition of azidomethyl methyl sulfide (AMMS) yields a transient S-methylthiaziridine which rapidly evolves to S-methyl-N-sulfenylmethanimine at 10 K. This species was detected by infrared matrix isolation spectroscopy. The mechanism of the photoreaction of AMMS has been investigated by a
Chemistry Letters (Jpn), 653-653 (1993)
[Mutagenic activity of chlorodimethylsulfide and some of its aniline derivatives].
M Vito et al.
Bollettino della Societa italiana di biologia sperimentale, 61(6), 917-923 (1985-06-30)
Synthesis, 276-276 (1994)

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