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  2. 2-(5-chloro-2,4-difluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

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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)-

2-(5-chloro-2,4-difluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

CC1(C)OB(OC1(C)C)c1cc(Cl)c(cc1F)F Request for Quotation
Chemical Name: 2-(5-chloro-2,4-difluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS Number: 1073354-65-0
Product Number: AG007ENG(AGN-PC-0786LG)
Synonyms:
MDL No:
Molecular Formula: C12H14BClF2O2
Molecular Weight: 274.4992

Identification/Properties

Computed Properties
Molecular Weight:
274.499g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
274.074g/mol
Monoisotopic Mass:
274.074g/mol
Topological Polar Surface Area:
18.5A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
311
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 compound 2-(5-Chloro-2,4-difluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is widely utilized in chemical synthesis as a versatile building block. Its boron functionality enables it to participate in various cross-coupling reactions, particularly in Suzuki-Miyaura coupling reactions. By serving as a boronic acid precursor, this compound is crucial in the formation of carbon-carbon bonds, facilitating the synthesis of complex organic molecules such as pharmaceuticals, agrochemicals, and materials. Additionally, its unique fluorinated and chlorinated phenyl group enhances the reactivity and specificity of the compound in targeted synthesis pathways, making it an essential tool in modern organic chemistry.