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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)-

Sulfamic acid,N-[bis(methylthio)methylene]-, 2,2,2-trichloroethyl ester

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Chemical Name: Sulfamic acid,N-[bis(methylthio)methylene]-, 2,2,2-trichloroethyl ester
CAS Number: 882739-46-0
Product Number: AG003U6C(AGN-PC-0VKF7X)
Synonyms:
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Molecular Formula:
Molecular Weight:

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Chemical Structure


S,S-Dimethyl N-(2,2,2-trichloroethoxysulfonyl)carbonimidodithionate is a versatile reagent widely utilized in chemical synthesis for its unique functional group reactivity. This compound is commonly employed as a sulfur transfer agent in organic transformations, enabling efficient sulfur incorporation into various organic molecules. In particular, it is frequently utilized in the synthesis of sulfur-containing compounds such as sulfoxides, sulfones, and sulfonamides. Additionally, this reagent is known for its ability to selectively transfer the sulfur atom to specific functional groups under mild reaction conditions, making it a valuable tool in the development of complex molecular structures. The use of S,S-Dimethyl N-(2,2,2-trichloroethoxysulfonyl)carbonimidodithionate in chemical synthesis offers chemists a reliable and effective method for the introduction of sulfur functionality in target molecules, ultimately aiding in the synthesis of diverse organic compounds with varied applications.