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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)-

4-Cyanomethoxyphenylboronic acid

OB(c1ccc(cc1)OCC#N)O Request for Quotation
Chemical Name: 4-Cyanomethoxyphenylboronic acid
CAS Number: 947533-23-5
Product Number: AG00IIIH(AGN-PC-03HPL8)
Synonyms:
MDL No:
Molecular Formula: C8H8BNO3
Molecular Weight: 176.9650

Identification/Properties

Computed Properties
Molecular Weight:
176.966g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
177.06g/mol
Monoisotopic Mass:
177.06g/mol
Topological Polar Surface Area:
73.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
193
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


B-[4-(Cyanomethoxy)phenyl]boronic acid, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound is often utilized as a key reagent in Suzuki-Miyaura cross-coupling reactions, where it serves as a source of the boron moiety for the formation of carbon-carbon bonds. By participating in this palladium-catalyzed coupling reaction, $name$ enables the efficient construction of complex organic molecules with high precision and selectivity. Furthermore, its unique structure incorporating a cyano-methoxyphenyl group imparts specific properties to the resulting products, making it valuable for the synthesis of pharmaceuticals, agrochemicals, and advanced materials. In addition to its use in cross-coupling reactions, $name$ can also be employed in other synthetic transformations such as direct arylation, borylation, and functionalization of aromatic compounds. Its compatibility with a wide range of functional groups and its ability to facilitate the synthesis of diverse chemical structures make $name$ a valuable tool in modern organic chemistry.