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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-fluoro-2-(trifluoromethyl)phenol

Fc1ccc(c(c1)C(F)(F)F)O Request for Quotation
Chemical Name: 4-fluoro-2-(trifluoromethyl)phenol
CAS Number: 130047-19-7
Product Number: AG000TXI(AGN-PC-0JS8HU)
Synonyms:
MDL No: MFCD00061290
Molecular Formula: C7H4F4O
Molecular Weight: 180.0997

Identification/Properties

Properties
MP:
50-54℃
BP:
169.3°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
180.102g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
0
Exact Mass:
180.02g/mol
Monoisotopic Mass:
180.02g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
156
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-Fluoro-2-(trifluoromethyl)phenol, also known as $name$, is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. In organic chemistry, this compound serves as a valuable building block for the construction of various functional molecules due to its ability to undergo diverse chemical transformations.One key application of 4-Fluoro-2-(trifluoromethyl)phenol in chemical synthesis is its role as a key intermediate in the production of pharmaceuticals and agrochemicals. Its trifluoromethyl group provides increased lipophilicity and stability to the resulting compounds, enhancing their biological activity and pharmacokinetic properties. Additionally, the fluoro substituent enables selective functionalization reactions, facilitating the synthesis of complex organic molecules with precise stereochemical control.Furthermore, 4-Fluoro-2-(trifluoromethyl)phenol finds utility in the preparation of advanced materials, including polymers, dyes, and specialty chemicals. Its versatile reactivity allows for the introduction of fluorine-containing moieties into organic frameworks, leading to enhanced material properties such as thermal stability, chemical resistance, and optical characteristics.Overall, 4-Fluoro-2-(trifluoromethyl)phenol plays a crucial role in modern chemical synthesis, enabling the efficient and selective construction of diverse compounds with tailored functionalities for applications in pharmaceuticals, materials science, and other industrial sectors.