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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)-

Selenious acid, zinc salt (1:1)

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Chemical Name: Selenious acid, zinc salt (1:1)
CAS Number: 13597-46-1
Product Number: AG003VE9(AGN-PC-0PKRZW)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Properties
Storage:
Room Temperature;Keep in dry area;
Form:
Solid

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Zinc selenite (ZnSeO3) is a versatile compound that finds widespread application in chemical synthesis. In organic chemistry, it is often utilized as a catalyst in various reactions due to its unique properties. Zinc selenite can act as a Lewis acid catalyst, facilitating the formation of carbon-carbon and carbon-heteroatom bonds in a wide range of organic transformations. Its ability to activate certain functional groups makes it a valuable tool in the synthesis of complex molecules. Additionally, zinc selenite can also function as a mediator in oxidation-reduction reactions, enabling the conversion of substrates into valuable products with high efficiency. Overall, the diverse reactivity and catalytic properties of zinc selenite make it a valuable asset in the toolkit of synthetic chemists seeking to develop novel compounds and materials.