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38695-60-2

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38695-60-2 Usage

General Description

2-METHYLSULFONYLTHIOPHENE is a chemical compound with the molecular formula C5H8OS2. It is a member of the thiophene family and contains a methylsulfonyl group attached to the thiophene ring. 2-METHYLSULFONYLTHIOPHENE is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It has a strong odor and is known to be a potential irritant to the skin, eyes, and respiratory system. 2-METHYLSULFONYLTHIOPHENE is also used in the manufacturing of various organic electronic devices and materials due to its unique electronic properties, making it a versatile and important chemical in the research and industrial sectors.

Check Digit Verification of cas no

The CAS Registry Mumber 38695-60-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,6,9 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 38695-60:
(7*3)+(6*8)+(5*6)+(4*9)+(3*5)+(2*6)+(1*0)=162
162 % 10 = 2
So 38695-60-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H6O2S2/c1-9(6,7)5-3-2-4-8-5/h2-4H,1H3

38695-60-2 Well-known Company Product Price

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  • Alfa Aesar

  • (B20940)  2-(Methylsulfonyl)thiophene, 97%   

  • 38695-60-2

  • 1g

  • 1326.0CNY

  • Detail
  • Alfa Aesar

  • (B20940)  2-(Methylsulfonyl)thiophene, 97%   

  • 38695-60-2

  • 5g

  • 3172.0CNY

  • Detail

38695-60-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-METHYLSULFONYLTHIOPHENE

1.2 Other means of identification

Product number -
Other names methyl thien-2-yl sulfone

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:38695-60-2 SDS

38695-60-2Relevant articles and documents

High Chemoselectivity in the Construction of Aryl Methyl Sulfones via an Unexpected C-S Bond Formation between Sulfonylhydrazides and Dimethyl Phosphite

Liu, Teng,Yu, Shiwen,Shen, Xiang,Li, Yixian,Liu, Jianjun,Huang, Chao,Cheng, Feixiang

, p. 153 - 160 (2021/10/04)

A highly chemoselective route to aryl methyl sulfones via an unexpected C S bond formation between sulfonylhydrazides and dimethyl phosphite catalyzed by NaI under mild conditions has been established. This transformation provides an alternative and metal-free pathway to acquire various aryl methyl sulfones in good to excellent yields. Notably, dimethyl phosphite was employed as a stable and readily available alkyl source.

Preparation method of methyl sulfone compound

-

Paragraph 0005; 0031, (2021/02/24)

The invention discloses a synthesis method of a methyl sulfone compound, which comprises the following steps: by using an iodinated compound as a substrate, adding a sulfite compound into the substrate, and using a 1, 4-dioxane solution as a solvent, heating under the protection of nitrogen under the actions of a silicon reagent, a phase transfer catalyst and a palladium catalyst to obtain a crudeproduct; then purifying the crude product, firstly filtering the crude product, and removing the solvent to obtain residues; carrying out silica gel column chromatography on the residues, leaching with eluent, and collecting effluent; combining the effluent containing the product; and concentrating the combined effluent to remove the solvent, and finally carrying out vacuum drying to obtain the target product. The method has the advantages of simple process flow, easiness in product purification, environmental safety and high yield.

Selective oxidation of (hetero)sulfides with molecular oxygen under clean conditions

Liu, Kai-Jian,Deng, Ji-Hui,Yang, Jie,Gong, Shao-Feng,Lin, Ying-Wu,He, Jun-Yi,Cao, Zhong,He, Wei-Min

supporting information, p. 433 - 438 (2020/02/13)

The development of eco-friendly and switchable catalytic systems for the conversion of a sole raw-material into distinct high-value products is a particularly attractive concept and a daunting synthetic challenge. In the present work, the first example of efficient and selective oxidation of sulfides to sulfones and sulfoxides using molecular oxygen under clean conditions was established.

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