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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)-

Phenol, 2-fluoro-3-(trifluoromethyl)-

Oc1cccc(c1F)C(F)(F)F Request for Quotation
Chemical Name: Phenol, 2-fluoro-3-(trifluoromethyl)-
CAS Number: 207291-85-8
Product Number: AG002IXG(AGN-PC-0KK8ME)
Synonyms:
MDL No:
Molecular Formula: C7H4F4O
Molecular Weight: 180.0997

Identification/Properties

Properties
BP:
176.7 °C at 760 mmHg
Storage:
Room Temperature;
Form:
Liquid
Refractive Index:
n20/D 1.443(lit.)
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H312-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Fluoro-3-(trifluoromethyl)phenol, also known as $name$, is a versatile chemical compound widely used in chemical synthesis. This compound is valued for its unique properties that make it a valuable building block in the development of various pharmaceuticals, agrochemicals, and advanced materials. In chemical synthesis, $name$ serves as a key reagent in the production of complex molecules through its ability to undergo various transformations and functionalization reactions. Its fluoro and trifluoromethyl substituents enable precise control over the reactivity and selectivity of reactions, making it a powerful tool for synthetic chemists. $name$ is particularly prized for its role in the synthesis of fluorinated compounds, which are increasingly important in drug discovery and materials science due to their enhanced properties. By incorporating 2-Fluoro-3-(trifluoromethyl)phenol into chemical reactions, researchers can access new and innovative pathways to create highly functionalized molecules with improved pharmacological, biological, or physical characteristics.