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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)-

Borate(1-), hydrotriphenyl-, potassium, (T-4)-

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Chemical Name: Borate(1-), hydrotriphenyl-, potassium, (T-4)-
CAS Number: 99747-36-1
Product Number: AG003TXR(AGN-PC-0W9SNR)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

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Chemical Structure


Potassium triphenylborohydride solution is a versatile chemical reagent commonly used in organic synthesis. It serves as a powerful and selective reducing agent in a variety of chemical reactions. In particular, it is used for the reduction of carbonyl compounds, such as ketones and aldehydes, to their corresponding alcohols. This reagent is especially useful in the synthesis of complex organic molecules where precise control over the reduction process is crucial. Furthermore, Potassium triphenylborohydride solution is known for its mild reaction conditions, which helps to preserve sensitive functional groups present in the substrate molecule.Overall, its application in chemical synthesis offers a reliable method for the efficient and selective reduction of carbonyl compounds, making it a valuable tool in the arsenal of synthetic chemists.