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67764-21-0

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67764-21-0 Usage

General Description

1-(methoxysulfanyl)-4-methylbenzene, also known as p-methylthioanisole, is an organic compound with a molecular formula of C8H10OS. It is a colorless liquid with a faint, sweet, and fruity odor. 1-(methoxysulfanyl)-4-methylbenzene is commonly used in the fragrance and flavor industries as a scent additive for its unique and pleasant aroma. It can also be found in some food products as a flavoring agent. Additionally, 1-(methoxysulfanyl)-4-methylbenzene has been studied for its potential anti-inflammatory and antioxidant properties, making it a subject of interest for pharmaceutical and cosmetic applications. However, it is important to note that this chemical should be handled with care as it may cause skin irritation and could be harmful if swallowed or inhaled in large quantities.

Check Digit Verification of cas no

The CAS Registry Mumber 67764-21-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,7,6 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67764-21:
(7*6)+(6*7)+(5*7)+(4*6)+(3*4)+(2*2)+(1*1)=160
160 % 10 = 0
So 67764-21-0 is a valid CAS Registry Number.

67764-21-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methoxysulfanyl-4-methylbenzene

1.2 Other means of identification

Product number -
Other names Methyl-toluol-p-sulphenat

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:67764-21-0 SDS

67764-21-0Relevant articles and documents

Remarkably mild and simple preparation of sulfenate anions from β-sulfinylesters: A new route to enantioenriched sulfoxides

Caupene, Caroline,Boudou, Cedric,Perrio, Stephane,Metzner, Patrick

, p. 2812 - 2815 (2007/10/03)

(Chemical Equation Presented) A general, efficient, and experimentally simple method for the generation of sulfenate salts has been developed using β-sulfmylesters as substrates. The process is based on a retro-Michael reaction, initiated by deprotonation at low temperature. Upon treatment with alkyl halides, the liberated sulfenates are subsequently converted into sulfoxides in good to excellent yield. Extension of the methodology to an unprecedented access to nonracemic sulfoxides by introduction of an enantiopure ligand, (-)-sparteine, is also described.

REACTIONS OF DIARYL DISULFIDES WITH (N-CHLOROARENESULFONAMIDO)SODIUMS. N,N'-BIS(ARYLSULFONYL)-N-(ARYLTHIO)ARENESULFINIMIC AMIDES

Levchenko, E. S.,Pel'kis, N. P.

, p. 2447 - 2452 (2007/10/02)

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