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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)-

1-Propanesulfonothioic acid, S-propyl ester

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Chemical Name: 1-Propanesulfonothioic acid, S-propyl ester
CAS Number: 1113-13-9
Product Number: AG0038YZ(AGN-PC-0JSER1)
Synonyms:
MDL No:
Molecular Formula: C6H14O2S2
Molecular Weight: 182.3042

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Chemical Structure


1-Propanesulfonothioic acid, S-propyl ester is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in the production of various organic compounds, particularly in the pharmaceutical and agrochemical industries. With its unique structure and reactivity, the 1-Propanesulfonothioic acid, S-propyl ester allows for the introduction of sulfur-containing functional groups into complex molecules, enhancing their bioactivity and stability. In chemical synthesis, this compound is utilized as a thioester derivative, enabling the formation of new carbon-sulfur bonds and facilitating the creation of structurally diverse molecules with desired properties. Its compatibility with a wide range of reaction conditions makes it a valuable tool for organic chemists seeking to design and develop novel compounds for various applications.