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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-(4-morpholinyl)-5-pyrimidinyl]-

OB(c1cnc(nc1)N1CCOCC1)O Request for Quotation
Chemical Name: Boronic acid, [2-(4-morpholinyl)-5-pyrimidinyl]-
CAS Number: 870521-33-8
Product Number: AG008DPK(AGN-PC-07ZXB6)
Synonyms:
MDL No:
Molecular Formula: C8H12BN3O3
Molecular Weight: 209.0102

Identification/Properties

Computed Properties
Molecular Weight:
209.012g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
2
Exact Mass:
209.097g/mol
Monoisotopic Mass:
209.097g/mol
Topological Polar Surface Area:
78.7A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
194
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Morpholinopyrimidin-5-ylboronic acid is a versatile compound that finds wide application in chemical synthesis, particularly in the field of organic chemistry. This boronic acid derivative serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and materials.Due to its boronic acid functionality, 2-Morpholinopyrimidin-5-ylboronic acid is commonly employed in Suzuki-Miyaura cross-coupling reactions. In this reaction, the boronic acid group undergoes a palladium-catalyzed coupling with an organic halide or triflate, leading to the formation of a new carbon-carbon bond. This reaction is widely used in the construction of complex organic molecules and is a powerful tool in modern synthetic chemistry.Additionally, 2-Morpholinopyrimidin-5-ylboronic acid can also participate in other transformations such as Heck reactions, Sonogashira couplings, and Buchwald-Hartwig aminations. These versatile reactions allow for the introduction of the 2-morpholinopyrimidin-5-ylboronic acid moiety into a wide variety of molecular scaffolds, making it a valuable building block in the synthesis of diverse chemical compounds.Overall, the application of 2-Morpholinopyrimidin-5-ylboronic acid in chemical synthesis enables chemists to access novel molecules with potential pharmaceutical, agricultural, and materials applications.