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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-amino-3,5-difluoro-

OC(=O)c1cc(F)c(c(c1)F)N Request for Quotation
Chemical Name: Benzoic acid, 4-amino-3,5-difluoro-
CAS Number: 500577-99-1
Product Number: AG00DG7M(AGN-PC-0JP5YC)
Synonyms:
MDL No:
Molecular Formula: C7H5F2NO2
Molecular Weight: 173.1169

Identification/Properties

Computed Properties
Molecular Weight:
173.119g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
173.029g/mol
Monoisotopic Mass:
173.029g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
176
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


4-Amino-3,5-difluorobenzoic acid is a versatile compound widely utilized in chemical synthesis for its specific properties and reactivity. As a benzoic acid derivative, it serves as a key intermediate in the pharmaceutical industry, particularly in the synthesis of various biologically active compounds and pharmaceutical ingredients.This compound plays a crucial role in the development of new drugs and agrochemicals due to its ability to undergo various reactions and form diverse chemical structures. Its presence as a building block in organic synthesis enables the formation of complex molecules with specific functionalities.In organic chemistry, 4-Amino-3,5-difluorobenzoic acid is frequently employed in coupling reactions, such as amide bond formation, which is essential in peptide synthesis and pharmaceutical research. Additionally, its fluorine atoms confer unique properties that can enhance the biological activity of the final products.Furthermore, its amino group allows for further derivatization, enabling the introduction of other functional groups to modulate the compound's properties. This flexibility makes it a valuable component in custom synthesis and drug discovery efforts.Overall, the application of 4-Amino-3,5-difluorobenzoic acid in chemical synthesis underscores its significance as a key building block in the creation of novel compounds with diverse applications in medicinal chemistry and materials science.