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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-(dihydroxyboranyl)-2,3-difluorobenzoic acid

OB(c1ccc(c(c1F)F)C(=O)O)O Request for Quotation
Chemical Name: 4-(dihydroxyboranyl)-2,3-difluorobenzoic acid
CAS Number: 1029716-92-4
Product Number: AG008SUN(AGN-PC-0WA9IN)
Synonyms:
MDL No:
Molecular Formula: C7H5BF2O4
Molecular Weight: 201.9200

Identification/Properties

Computed Properties
Molecular Weight:
201.92g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
2
Exact Mass:
202.025g/mol
Monoisotopic Mass:
202.025g/mol
Topological Polar Surface Area:
77.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
226
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Borono-2,3-difluorobenzoic acid is a versatile compound commonly used in chemical synthesis due to its unique properties and reactivity. This compound serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and organic materials. Its boronic acid functionality allows for efficient cross-coupling reactions with aryl halides, making it an essential component in the formation of complex molecules. In addition, the presence of difluoromethyl groups enhances the compound's stability and can impart desirable properties to the final products. Overall, 4-Borono-2,3-difluorobenzoic acid plays a crucial role in the synthesis of diverse compounds with potential applications in the fields of medicine, agriculture, and materials science.