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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)-

(3,4-difluoro-2-formylphenyl)boronic acid

O=Cc1c(ccc(c1F)F)B(O)O Request for Quotation
Chemical Name: (3,4-difluoro-2-formylphenyl)boronic acid
CAS Number: 1451392-91-8
Product Number: AG01DDWW(AG01DDWW)
Synonyms:
MDL No:
Molecular Formula: C7H5BF2O3
Molecular Weight: 185.9206

Identification/Properties

Computed Properties
Molecular Weight:
185.921g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
186.03g/mol
Monoisotopic Mass:
186.03g/mol
Topological Polar Surface Area:
57.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
191
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 B-(3,4-Difluoro-2-formylphenyl)boronic acid is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In organic chemistry, this compound serves as a valuable building block for the preparation of various organic molecules and pharmaceuticals. Its boronic acid group allows for facile Suzuki-Miyaura cross-coupling reactions with aryl halides, enabling the formation of carbon-carbon bonds with high efficiency. Additionally, the difluoro-substituted phenyl and formyl groups add specific functionality to the molecule, enhancing its utility in drug discovery and material science. This compound's ability to participate in diverse chemical transformations makes it a valuable tool for synthetic chemists seeking to access complex molecular architectures.