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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)-

Boronic acid, (3-cyano-5-fluorophenyl)-

N#Cc1cc(F)cc(c1)B(O)O Request for Quotation
Chemical Name: Boronic acid, (3-cyano-5-fluorophenyl)-
CAS Number: 304858-67-1
Product Number: AG0030AS(AGN-PC-0435JJ)
Synonyms:
MDL No:
Molecular Formula: C7H5BFNO2
Molecular Weight: 164.9295

Identification/Properties

Properties
BP:
343.1°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
164.93g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
165.04g/mol
Monoisotopic Mass:
165.04g/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


3-Cyano-5-fluorophenylboronic acid is a versatile chemical reagent that finds widespread application in organic synthesis. Its unique chemical structure, containing a cyano group and a boronic acid moiety, imparts specific properties that make it valuable in the construction of complex organic molecules.In chemical synthesis, 3-Cyano-5-fluorophenylboronic acid serves as a key building block for the formation of various biologically active compounds and pharmaceuticals. Its boronic acid functionality allows for the formation of stable boronate esters through Suzuki-Miyaura cross-coupling reactions. This makes it an essential component in the synthesis of aryl cyanides, which are crucial intermediates in the pharmaceutical industry.Additionally, the cyano group present in 3-Cyano-5-fluorophenylboronic acid can undergo diverse chemical reactions, enabling the introduction of the cyano functionality into target molecules. This enables the synthesis of heterocyclic compounds, agrochemicals, and materials with specific properties.Overall, the strategic placement of both the cyano and boronic acid groups in 3-Cyano-5-fluorophenylboronic acid allows for precise control over the reactivity and functionality of the molecule, making it a valuable tool in modern organic synthesis.