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3708-04-1

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3708-04-1 Usage

General Description

2-Methylsulfonylacetophenone is a chemical compound with the molecular formula C10H12O2S. It is an organosulfur compound, specifically a ketone derivative, and is commonly used in organic synthesis as a reagent for various types of chemical reactions. It is known for its strong garlic-like odor and is often used as a flavoring agent in the food industry. Additionally, it has been studied for its potential anti-inflammatory and antioxidant properties, making it of interest for pharmaceutical and cosmetic applications. However, it is important to handle this chemical with caution due to its potential to cause skin and eye irritation and its flammable nature.

Check Digit Verification of cas no

The CAS Registry Mumber 3708-04-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,0 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3708-04:
(6*3)+(5*7)+(4*0)+(3*8)+(2*0)+(1*4)=81
81 % 10 = 1
So 3708-04-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O3S/c1-13(11,12)7-9(10)8-5-3-2-4-6-8/h2-6H,7H2,1H3

3708-04-1SDS

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-(Methylsulfonyl)acetophenone

1.2 Other means of identification

Product number -
Other names 2-methylsulfonyl-1-phenylethanone

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:3708-04-1 SDS

3708-04-1Relevant articles and documents

PREFERRED CONFORMATIONS OF METHYLTHIO-ACETONE AND -ACETOPHENONE, METHYLSULPHONYL-ACETONE AND -ACETOPHENONE, FROM MOLECULAR-MECHANICS AND DIPOLE-MOMENT TECHNIQUES

Lumbroso, H.,Bertin, D. M.,Olivato, P. R.,Bonfada, E.,Mondino, M. G.,Hase, Y.

, p. 113 - 122 (1989)

Preferred conformations for the title compounds are determined from calculated molecular-mechanics energies in the gaseous phase and analysis of the dipole moments measured in solvents of low dielectric permittivity.In all cases, the gauche conformer having the Me-S bond situated far away from the Me(-C) (or Ph(-C)) group, and nearly bisecting one of the C(=O)-C-H valleys, is predominant.

Oxidant-free C-H sulfonylation of enamides: Electrochemical synthesis of β-amidovinyl and carbonyl sulfones from sulfonyl hydrazide and enamides

Qi, Liang,Xiao, Linxia,Chen, Xi,Zhang, Ziyi,Shi, Qin,Chen, Jinkang

supporting information, (2021/12/17)

A mild, practical, eco-friendly and environmentally friendly electrochemical synthesis method of β-aminovinyl sulfone and carbonyl sulfones from sulfonyl hydrazide and enamides has been developed. This transformation only requires electrolytes and solvent, thus avoids transition metal catalysts, stoichiometric oxidant and base. Two different types of sulfone derivatives can be obtained only by changing the reaction solvent. This transformation also features mild conditions (room temperature, air), broad substrate scopes, and excellent stereoselectivities in mild to good yield.

Photosensitizer-free synthesis of β-keto sulfones: Via visible-light-induced oxysulfonylation of alkenes with sulfonic acids

Hong, Yun-Yun,Peng, Sha,Peng, Zhen,Tang, Shan-Shan,Xie, Long-Yong,Xu, Xiang-Qun,Yang, Li-Hua

supporting information, p. 4537 - 4541 (2021/05/31)

A practical and environment-friendly methodology for the construction of β-keto sulfones through visible-light induced direct oxysulfonylation of alkenes with sulfonic acids at ambient temperature under open-air conditions was developed. Most importantly, the reaction proceeded smoothly without the addition of any photocatalyst or strong oxidant, ultimately minimizing the production of chemical waste.

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