(+/-)-2-(methylsulfinyl)thiophene

Base Information

Chemical Name:(+/-)-2-(methylsulfinyl)thiophene
CAS No.:74166-42-0
Molecular Formula:C₅H₆OS₂
Molecular Weight:146.234
Hs Code.:

Synonyms:(+/-)-2-(methylsulfinyl)thiophene

Suppliers and Price of (+/-)-2-(methylsulfinyl)thiophene

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (+/-)-2-(methylsulfinyl)thiophene

Chemical Property:

Purity/Quality:

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Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of (+/-)-2-(methylsulfinyl)thiophene

There total 1 articles about (+/-)-2-(methylsulfinyl)thiophene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 3.0%

: 5780-36-9
2-(methylsulfanyl)thiophene

: 38695-60-2
Methyl-<2>thienylsulfon

: 74166-42-0
(+/-)-2-(methylsulfinyl)thiophene

Guidance literature:: With dihydrogen peroxide; In acetone; for 288h; Ambient temperature;
DOI:10.1007/BF00938722

Reference yield: 78.0%

: 29526-96-3
1-phenylcyclopropan-1-ol

: 74166-42-0
(+/-)-2-(methylsulfinyl)thiophene

: C₁₄H₁₄OS₂

Guidance literature:: With 2,2,3,3,3-pentafluoropropanoic anhydride; sodium 2,2,2-trifluoroacetate; In dichloromethane; at 20 ℃; for 8h; regioselective reaction; Inert atmosphere; Molecular sieve;
DOI:10.1021/acs.orglett.9b01908

Reference yield: 77.0%

: 623-13-2
4-methylphenyl methylsulfide

: 74166-42-0
(+/-)-2-(methylsulfinyl)thiophene

: 5-methylsulfanyl-2-thienyl 4-tolyl sulfide

Guidance literature:: 4-methylphenyl methylsulfide; (+/-)-2-(methylsulfinyl)thiophene; With trifluoromethylsulfonic anhydride; trifluoroacetic anhydride; In dichloromethane; at 25 ℃; for 0.5h; Schlenk technique; Inert atmosphere;

With ethanolamine; In dichloromethane; at 25 ℃; for 3h; regioselective reaction; Schlenk technique; Inert atmosphere;
DOI:10.1021/acs.orglett.7b02147