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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)-

Boronic acid, [2-(dimethylamino)-4-(phenylmethoxy)-5-pyrimidinyl]-

OB(c1cnc(nc1OCc1ccccc1)N(C)C)O Request for Quotation
Chemical Name: Boronic acid, [2-(dimethylamino)-4-(phenylmethoxy)-5-pyrimidinyl]-
CAS Number: 205672-21-5
Product Number: AG002AA2(AGN-PC-0NAT7E)
Synonyms:
MDL No:
Molecular Formula: C13H16BN3O3
Molecular Weight: 273.0954

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
273.099g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
5
Exact Mass:
273.128g/mol
Monoisotopic Mass:
273.128g/mol
Topological Polar Surface Area:
78.7A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
288
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Benzyloxy-2-(dimethylamino)pyrimidine-5-boronic acid is a versatile compound widely used in chemical synthesis. With its unique structure and properties, this compound is specifically valued for its ability to participate in various palladium-catalyzed cross-coupling reactions. In organic synthesis, 4-Benzyloxy-2-(dimethylamino)pyrimidine-5-boronic acid acts as a crucial building block for the construction of complex molecules and pharmaceutical intermediates. Its boronic acid functionality enables it to undergo Suzuki-Miyaura coupling reactions, allowing for the introduction of aryl or vinyl groups under mild reaction conditions. This capability makes it a valuable tool in the synthesis of biaryl compounds, which are prevalent in medicinal chemistry and material science. Furthermore, the dimethylamino group can serve as a directing or activating group in various transformations, enabling selective functionalization at specific positions within the molecule. This level of control is essential in designing efficient synthetic routes and obtaining high yields of the desired products.Overall, the application of 4-Benzyloxy-2-(dimethylamino)pyrimidine-5-boronic acid in chemical synthesis demonstrates its significance as a key reagent for the construction of diverse molecular architectures with precise control over regio- and stereochemistry.