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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-2,6-difluorophenyl)boronic acid

OB(c1c(F)ccc(c1F)Cl)O Request for Quotation
Chemical Name: (3-chloro-2,6-difluorophenyl)boronic acid
CAS Number: 1031226-45-5
Product Number: AG003BRO(AGN-PC-0L170Y)
Synonyms:
MDL No:
Molecular Formula: C6H4BClF2O2
Molecular Weight: 192.3556

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
192.353g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
191.996g/mol
Monoisotopic Mass:
191.996g/mol
Topological Polar Surface Area:
40.5A^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

NMR Spectrum

Other Analytical Data

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Chemical Structure


(3-Chloro-2,6-difluorophenyl)boronic acid is a versatile compound widely used in chemical synthesis as a key building block for the preparation of various organic molecules. This boronic acid derivative serves as an important intermediate in Suzuki-Miyaura cross-coupling reactions, allowing for the efficient formation of carbon-carbon bonds under mild reaction conditions. Its unique chemical properties make it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Furthermore, (3-Chloro-2,6-difluorophenyl)boronic acid exhibits excellent reactivity and compatibility with a wide range of functional groups, making it a valuable asset in the toolbox of synthetic chemists.