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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)-

[1,3-bis(methoxymethyl)-2,4-dioxopyrimidin-5-yl]boronic acid

COCn1cc(B(O)O)c(=O)n(c1=O)COC Request for Quotation
Chemical Name: [1,3-bis(methoxymethyl)-2,4-dioxopyrimidin-5-yl]boronic acid
CAS Number: 1256346-16-3
Product Number: AG000O1F(AGN-PC-09PZ08)
Synonyms:
MDL No:
Molecular Formula: C8H13BN2O6
Molecular Weight: 244.0096

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound $name$ is a versatile boronic acid derivative that finds wide application in chemical synthesis. As a member of the pyrimidinylboronic acid family, $name$ is particularly valued for its role as a key building block in the formation of complex organic molecules. In synthetic chemistry, it serves as a valuable reagent for the Suzuki-Miyaura cross-coupling reaction, a widely utilized method for the construction of carbon-carbon bonds. By participating in this reaction, $name$ facilitates the creation of structurally intricate compounds with diverse functionalities, making it an indispensable tool for the preparation of pharmaceuticals, agrochemicals, and advanced materials. Furthermore, its unique structural features provide chemists with opportunities to explore new pathways in the design and synthesis of novel molecules with tailored properties and applications.