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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)-

N-1-Butyl-1-demethylethyl Torsemide

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Chemical Name: N-1-Butyl-1-demethylethyl Torsemide
CAS Number: 160972-33-8
Product Number: AG00ADNX(AGN-PC-0WOZSB)
Synonyms:
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Molecular Formula:
Molecular Weight:

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Chemical Structure


$Name$ is a potent diuretic that has a variety of applications in chemical synthesis. One prominent use of N-1-Butyl-1-demethylethyl Torsemide is as a reagent in the development of novel pharmaceutical compounds. Its unique structure and properties make it a valuable tool in the synthesis of biologically active molecules, particularly in the context of drug discovery and development. Furthermore, N-1-Butyl-1-demethylethyl Torsemide can also serve as a key building block in the creation of specialized organic compounds with specific functionalities. Its versatility and reactivity make it a valuable resource for chemists and researchers seeking to explore new avenues in synthetic chemistry.