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7341-24-4

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7341-24-4 Usage

General Description

2-Methylbenzyl mercaptan is a chemical compound with the formula C8H10S. It is a colorless to pale yellow liquid with a pungent, skunk-like odor. 2-METHYLBENZYL MERCAPTAN is primarily used as a flavoring agent and odorant in the food and beverage industry, imparting a sulfur-like, cooked onion aroma. It is also used in the production of fragrances and as a scent additive in natural gas to alert individuals of potentially dangerous leaks. Although it is considered to have a low toxicity, it can cause skin and eye irritation, and should be handled with care.

Check Digit Verification of cas no

The CAS Registry Mumber 7341-24-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,4 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7341-24:
(6*7)+(5*3)+(4*4)+(3*1)+(2*2)+(1*4)=84
84 % 10 = 4
So 7341-24-4 is a valid CAS Registry Number.

7341-24-4 Well-known Company Product Price

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  • Alfa Aesar

  • (A15816)  2-Methylbenzyl mercaptan, 97%   

  • 7341-24-4

  • 5g

  • 460.0CNY

  • Detail
  • Alfa Aesar

  • (A15816)  2-Methylbenzyl mercaptan, 97%   

  • 7341-24-4

  • 25g

  • 1823.0CNY

  • Detail
  • Alfa Aesar

  • (A15816)  2-Methylbenzyl mercaptan, 97%   

  • 7341-24-4

  • 100g

  • 6529.0CNY

  • Detail

7341-24-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-methylphenyl)methanethiol

1.2 Other means of identification

Product number -
Other names o-methylbenzyl mercaptan

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:7341-24-4 SDS

7341-24-4Relevant articles and documents

Nonenzymatic Dynamic Kinetic Resolution of in situ Generated Hemithioacetals: Access to 1,3-Disubstituted Phthalans

Nath, Utpal,Chowdhury, Deepan,Pan, Subhas Chandra

, p. 1628 - 1633 (2018/03/21)

The first nonenzymatic DKR reaction of hemithioacetals is developed. Hemithioacetals were formed in situ via thiol addition and subsequently underwent an intramolecular oxa-Michael reaction. The scope of the reaction was quite broad ranging from aliphatic to aromatic substituents and 1,3-disubstituted-1,3-dihyroisobenzofuran products were obtained in good yields with moderate diastereoselectivities and high enantioselectivities. (Figure presented.).

Reductive opening of thiophthalan: A new route to functionalized sulfur-containing compounds

Almena, Juan,Foubelo, Francisco,Yus, Miguel

, p. 1859 - 1862 (2007/10/03)

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