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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)-

Boronicacid, B-[4-(1-methylethyl)-5-pyrimidinyl]-

CC(c1ncncc1B(O)O)C Request for Quotation
Chemical Name: Boronicacid, B-[4-(1-methylethyl)-5-pyrimidinyl]-
CAS Number: 913835-27-5
Product Number: AG003BW6(AGN-PC-0713JZ)
Synonyms:
MDL No:
Molecular Formula: C7H11BN2O2
Molecular Weight: 165.9854

Identification/Properties

Properties
MP:
104-109
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
165.987g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
166.091g/mol
Monoisotopic Mass:
166.091g/mol
Topological Polar Surface Area:
66.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
143
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The chemical compound (4-Isopropylpyrimidin-5-yl)boronic acid, also known as $name$, is a versatile tool in chemical synthesis. This boronic acid derivative is commonly used as a building block in organic chemistry reactions, particularly in the field of metal-catalyzed cross-coupling reactions.In chemical synthesis, (4-Isopropylpyrimidin-5-yl)boronic acid serves as a valuable source of the pyrimidine moiety, providing a platform for the introduction of various functional groups. It can participate in Suzuki-Miyaura cross-coupling reactions, where it reacts with aryl or vinyl halides under the catalysis of palladium to form biaryl or bivinyl compounds. This reaction is widely utilized in the pharmaceutical industry and academic research for the formation of complex molecules and drug discovery.Moreover, (4-Isopropylpyrimidin-5-yl)boronic acid can be employed in other types of coupling reactions, such as palladium-catalyzed Buchwald-Hartwig amination, Sonogashira coupling, and Stille coupling, expanding its utility in the synthesis of diverse organic compounds. Its compatibility with various functional groups and the mild reaction conditions make it a valuable tool for chemists working on the development of new materials, pharmaceuticals, and agrochemicals.