1. Home
  2. 3,5-Difluoro-4-methylphenylboronic acid

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

3,5-Difluoro-4-methylphenylboronic acid

OB(c1cc(F)c(c(c1)F)C)O Request for Quotation
Chemical Name: 3,5-Difluoro-4-methylphenylboronic acid
CAS Number: 1621332-09-9
Product Number: AG00HYPZ(AGN-00HYKF)
Synonyms:
MDL No:
Molecular Formula: C7H7BF2O2
Molecular Weight: 171.9371

Identification/Properties

Computed Properties
Molecular Weight:
171.938g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
172.051g/mol
Monoisotopic Mass:
172.051g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
144
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

Request for Quotation

Customer Feedback

Chemical Structure


$Name$ is a highly versatile chemical compound that plays a crucial role in chemical synthesis. One of its main applications is as a key building block in the preparation of pharmaceuticals, agrochemicals, and materials. 3,5-Difluoro-4-methylphenylboronic acid's unique structure and reactivity make it an essential tool for chemists seeking to create specific molecular structures with precision. By incorporating $name$ into synthetic pathways, researchers can access a wide range of compounds that may not be readily available through traditional methods. Its use in Suzuki-Miyaura cross-coupling reactions, for example, allows for the selective formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules. Furthermore, $name$ can also serve as a valuable ligand in transition metal-catalyzed processes, facilitating the efficient construction of intricate molecular architectures. In summary, the strategic utilization of 3,5-Difluoro-4-methylphenylboronic acid in chemical synthesis enables chemists to unlock new possibilities and accelerate the discovery of novel compounds with diverse applications.