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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-Chloro-2,6-difluorophenylboronic acid

OB(c1c(F)cc(cc1F)Cl)O Request for Quotation
Chemical Name: 4-Chloro-2,6-difluorophenylboronic acid
CAS Number: 925911-61-1
Product Number: AG0063VL(AGN-PC-0L9ZPU)
Synonyms:
MDL No:
Molecular Formula: C6H4BClF2O2
Molecular Weight: 192.3556

Identification/Properties

Properties
MP:
149-151°C
Storage:
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:
149
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


Boronic acid, B-(4-chloro-2,6-difluorophenyl)-, is a versatile compound widely used in chemical synthesis as a key reagent in the formation of carbon-carbon bonds. This particular boronic acid derivative serves as a valuable building block for the construction of various pharmaceuticals, agrochemicals, and materials due to its unique reactivity and functionality. In organic synthesis, it can participate in Suzuki-Miyaura cross-coupling reactions with aryl halides, enabling the selective formation of complex molecular structures. Furthermore, this boronic acid derivative has found application in the preparation of fluorescent dyes, liquid crystals, and other advanced materials, highlighting its significance in the synthesis of diverse compounds with specific properties and functionalities.