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275956

Sigma-Aldrich

Methyl p-tolyl sulfide

99%

Synonym(s):

4-(Methylthio)toluene

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About This Item

Linear Formula:
CH3C6H4SCH3
CAS Number:
623-13-2
Molecular Weight:
138.23
EC Number:
210-773-8
MDL number:
MFCD00008560
UNSPSC Code:
12352100
PubChem Substance ID:
24856683
NACRES:
NA.22

Quality Level

200

Assay

99%

form

liquid

refractive index

n20/D 1.573 (lit.)

bp

52-54 °C/1 mmHg (lit.)

density

1.027 g/mL at 25 °C (lit.)

SMILES string

CSc1ccc(C)cc1

InChI

1S/C8H10S/c1-7-3-5-8(9-2)6-4-7/h3-6H,1-2H3

InChI key

VHILIAIEEYLJNA-UHFFFAOYSA-N

General description

Aerobic oxidation of methyl p-tolyl sulfide catalyzed by a heteroscorpionate Ru(II)-aqua complex has been reported. Chloroperoxidase catalyzed oxidation of methyl p-tolyl sulfide has been reported.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

185.0 °F - closed cup

Flash Point(C)

85 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

275956-25G:
275956-5G:
275956-BULK:
275956-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
BGBC3542V
MKBD5895V
MKBH8783V
MKBD5895
12120LH

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Sigma-Aldrich

T39802

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Chloroperoxidase and hydrogen peroxide: An efficient system for enzymatic enantioselective sulfoxidations
Colonna S, et al.
Tetrahedron Asymmetry, 3(1), 95-106 (1992)
My Hang V Huynh et al.
Journal of the American Chemical Society, 125(2), 308-309 (2003-01-09)
fac-[RuII(Cl)(dpp)(L3)]+ (L3 = tris(pyrid-2-yl)methoxymethane (tpmm) = [1A]+ and tris(pyrid-2-yl)pentoxymethane (tppm) = [1B]+ and dpp = di(pyrazol-1-yl)propane) rapidly undergo ligand substitution with water to form fac-[RuII(H2O)(dpp)(L3)]2+ (L3 = tpmm = [2A]2+ and tppm = [2B]2+). In the structure of [2A]2+, the
Vasiliy Yu Evtushok et al.
Frontiers in chemistry, 7, 858-858 (2020-01-11)
In this work, we elaborated heterogeneous catalysts on the basis of the Venturello complex [PO4{WO(O2)2}4]3- (PW4) and nitrogen-free or nitrogen-doped carbon nanotubes (CNTs or N-CNTs) for epoxidation of alkenes and sulfoxidation of thioethers with aqueous hydrogen peroxide. Catalysts PW4/CNTs and

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