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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

S-(1,1-Dioxothiolan-3-yl) ethanethioate

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Chemical Name: S-(1,1-Dioxothiolan-3-yl) ethanethioate
CAS Number: 201990-25-2
Product Number: AG00I3S3(AGN-PC-0WAF0F)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

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Chemical Structure


S-(Tetrahydro-1,1-dioxido-3-thienyl) ethanethioate, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in the creation of various organic molecules due to its unique structure and reactivity. In chemical synthesis, S-(Tetrahydro-1,1-dioxido-3-thienyl) ethanethioate can act as a thioester, providing a sulfur atom that can participate in nucleophilic substitution reactions. It can also serve as a protecting group for alcohols or a precursor for thiol derivatives. Additionally, this compound can be used as a reagent in the formation of carbon-sulfur bonds, which are essential in the synthesis of many pharmaceuticals, agrochemicals, and natural products. Overall, the application of S-(Tetrahydro-1,1-dioxido-3-thienyl) ethanethioate in chemical synthesis enables the efficient and strategic construction of complex organic molecules with diverse functionalities.