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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)-

(6-chloro-4-methylpyridin-3-yl)boronic acid

OB(c1cnc(cc1C)Cl)O Request for Quotation
Chemical Name: (6-chloro-4-methylpyridin-3-yl)boronic acid
CAS Number: 913836-08-5
Product Number: AG00GSKG(AGN-PC-07133B)
Synonyms:
MDL No:
Molecular Formula: C6H7BClNO2
Molecular Weight: 171.3893

Identification/Properties

Computed Properties
Molecular Weight:
171.387g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
171.026g/mol
Monoisotopic Mass:
171.026g/mol
Topological Polar Surface Area:
53.4A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
136
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


Boronic acid B-(6-chloro-4-methyl-3-pyridinyl) is a versatile compound widely utilized in chemical synthesis as a key building block. This particular boronic acid derivative is valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in a controlled and efficient manner. Its unique structure containing the pyridine ring with a chlorine and methyl group allows for specific interactions and selective reactions with various organic substrates. By serving as a critical reagent in the synthesis of complex molecules, this boronic acid compound plays a crucial role in the development of pharmaceuticals, agrochemicals, and materials with tailored properties. Its significance in modern synthetic chemistry lies in its capacity to facilitate the construction of intricate molecular structures with high precision and reliability.