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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)-

2-Furancarboxylic acid, 5-[2-(trifluoromethyl)phenyl]-

OC(=O)c1ccc(o1)c1ccccc1C(F)(F)F Request for Quotation
Chemical Name: 2-Furancarboxylic acid, 5-[2-(trifluoromethyl)phenyl]-
CAS Number: 92973-24-5
Product Number: AG00GYDN(AGN-PC-0JUAXI)
Synonyms:
MDL No:
Molecular Formula: C12H7F3O3
Molecular Weight: 256.1774

Identification/Properties

Computed Properties
Molecular Weight:
256.18g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
2
Exact Mass:
256.035g/mol
Monoisotopic Mass:
256.035g/mol
Topological Polar Surface Area:
50.4A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
316
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:
Danger
UN#:
2811
Hazard Statements:
H301-H315-H317-H319-H335
Precautionary Statements:
P261-P280-P301+P310-P305+P351+P338
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-(2-(Trifluoromethyl)phenyl)furan-2-carboxylic acid, a versatile compound in chemical synthesis, serves as a crucial building block in the creation of various organic molecules. With its unique structure and functional groups, this acid is particularly valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. By utilizing the reactivity of the carboxylic acid and the trifluoromethyl group, chemists can efficiently introduce this scaffold into complex molecular structures, allowing for the synthesis of diverse compounds with desirable properties and functions. Additionally, the furan ring provides additional opportunities for structural modification and diversification within the molecule, enabling the production of novel chemicals with enhanced biological or physical characteristics. In essence, the strategic incorporation of 5-(2-(Trifluoromethyl)phenyl)furan-2-carboxylic acid in chemical processes enables the synthesis of valuable compounds with potential applications in various industries.