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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)-

Benzoic acid, 4-bromo-2,5-difluoro-

Fc1cc(C(=O)O)c(cc1Br)F Request for Quotation
Chemical Name: Benzoic acid, 4-bromo-2,5-difluoro-
CAS Number: 28314-82-1
Product Number: AG00C3W5(AGN-PC-0JWKYR)
Synonyms:
MDL No:
Molecular Formula: C7H3BrF2O2
Molecular Weight: 236.9983

Identification/Properties

Properties
MP:
163-164°C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
237g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
235.928g/mol
Monoisotopic Mass:
235.928g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
188
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Bromo-2,5-difluorobenzoic acid is a versatile compound frequently employed in chemical synthesis due to its valuable properties and reactivity. This compound serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and materials. Its unique structure enables it to participate in a range of reactions, facilitating the formation of intricate molecular structures. In organic synthesis, 4-Bromo-2,5-difluorobenzoic acid is utilized as a key intermediate for the preparation of more complex molecules through processes such as esterification, amidation, and Suzuki-Miyaura coupling reactions. Its bromine and fluorine substituents confer specific characteristics to the resulting products, enhancing their biological activity or material properties. The use of 4-Bromo-2,5-difluorobenzoic acid in chemical synthesis underscores its significance as an indispensable component in the creation of innovative compounds with diverse applications.