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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-(5-chloro-2-methoxy-3-pyridinyl)-

COc1ncc(cc1B(O)O)Cl Request for Quotation
Chemical Name: Boronicacid, B-(5-chloro-2-methoxy-3-pyridinyl)-
CAS Number: 943153-22-8
Product Number: AG005Z7O(AGN-PC-078JP1)
Synonyms:
MDL No: MFCD04114579
Molecular Formula: C6H7BClNO3
Molecular Weight: 187.3887

Identification/Properties

Properties
MP:
148-152°C
BP:
353.1°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
187.386g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
187.021g/mol
Monoisotopic Mass:
187.021g/mol
Topological Polar Surface Area:
62.6A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
149
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (5-Chloro-2-methoxypyridin-3-yl)boronic acid is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. This boronic acid derivative serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and functional materials.Its application in cross-coupling reactions, particularly Suzuki-Miyaura coupling, is noteworthy. When coupled with suitable aryl or vinyl halides, this boronic acid facilitates the formation of C-C bonds, enabling the synthesis of complex organic molecules. Additionally, its compatibility with various reaction conditions and broad functional group tolerance make it a preferred reagent in the construction of diverse chemical structures.Furthermore, the presence of the electron-withdrawing chloro and methoxy substituents on the pyridine ring enhances the stability and selectivity of the boronic acid, making it an ideal candidate for challenging transformations in organic synthesis. Overall, the (5-Chloro-2-methoxypyridin-3-yl)boronic acid stands out as a valuable tool for chemists seeking efficient routes to novel compounds with potential applications in medicinal chemistry and materials science.