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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)-

(3-chloro-5-cyanophenyl)boronic acid

N#Cc1cc(Cl)cc(c1)B(O)O Request for Quotation
Chemical Name: (3-chloro-5-cyanophenyl)boronic acid
CAS Number: 915763-60-9
Product Number: AG00GSWI(AGN-PC-0AM075)
Synonyms:
MDL No:
Molecular Formula: C7H5BClNO2
Molecular Weight: 181.3841

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
181.382g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
181.01g/mol
Monoisotopic Mass:
181.01g/mol
Topological Polar Surface Area:
64.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
203
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


The (3-Chloro-5-cyanophenyl)boronic acid is a versatile building block in chemical synthesis, commonly utilized in organic reactions to introduce the cyanophenyl group into various target molecules. This compound serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials due to its ability to participate in Suzuki-Miyaura cross-coupling reactions. By engaging in these coupling reactions with appropriate partners, (3-Chloro-5-cyanophenyl)boronic acid enables the formation of biaryl compounds with high efficiency and selectivity. Furthermore, its boronic acid functionality allows for further derivatization through classic Suzuki, Heck, or Chan-Lam coupling reactions, expanding the scope of its applications in the realm of chemical synthesis.