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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)-

Benzeneacetic acid, 3,5-difluoro-a-hydroxy-

OC(c1cc(F)cc(c1)F)C(=O)O Request for Quotation
Chemical Name: Benzeneacetic acid, 3,5-difluoro-a-hydroxy-
CAS Number: 132741-31-2
Product Number: AG00113S(AGN-PC-0PJST0)
Synonyms:
MDL No:
Molecular Formula: C8H6F2O3
Molecular Weight: 188.1282

Identification/Properties

Properties
MP:
135-139 °C(lit.)
BP:
306.5°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
188.13g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
188.029g/mol
Monoisotopic Mass:
188.029g/mol
Topological Polar Surface Area:
57.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
188
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3,5-Difluoromandelic acid is a versatile compound widely used in chemical synthesis. Its unique molecular structure makes it a valuable building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials. In organic synthesis, 3,5-Difluoromandelic acid serves as a key intermediate for the preparation of more complex molecules through functional group transformations and derivatization reactions. Its fluorinated motif imparts distinct properties to the final products, enhancing their biological activity or material characteristics. The strategic incorporation of 3,5-Difluoromandelic acid into molecular scaffolds enables chemists to access a diverse array of compounds with tailored properties for specific applications in drug discovery, materials science, and other areas of research.