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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-cyclopropylpyridin-3-yl)boronic acid

OB(c1ccc(nc1)C1CC1)O Request for Quotation
Chemical Name: (6-cyclopropylpyridin-3-yl)boronic acid
CAS Number: 1253055-87-6
Product Number: AG000NGJ(AGN-PC-09QWD5)
Synonyms:
MDL No:
Molecular Formula: C8H10BNO2
Molecular Weight: 162.9815

Identification/Properties

Computed Properties
Molecular Weight:
162.983g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
163.08g/mol
Monoisotopic Mass:
163.08g/mol
Topological Polar Surface Area:
53.4A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
161
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#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(6-Cyclopropylpyridin-3-yl)boronic acid, also known as $name$, is a versatile compound utilized in chemical synthesis for various reactions due to its boronic acid functionality. In organic chemistry, this compound serves as a valuable building block in the formation of carbon-carbon and carbon-heteroatom bonds through Suzuki-Miyaura cross-coupling reactions. This reaction involves the coupling of an aryl or vinyl boronic acid with a halide or pseudohalide organic substrate catalyzed by a palladium complex, resulting in the formation of biaryl or vinyl-heteroatom compounds. Additionally, (6-Cyclopropylpyridin-3-yl)boronic acid finds application in transition metal-catalyzed transformations, such as palladium-catalyzed C-H activation reactions, enabling the selective functionalization of aromatic and heteroaromatic compounds. Its unique structural features make it a valuable tool for the efficient construction of complex molecules in organic synthesis.