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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)-

Benzenemethanol, 3-(trifluoromethyl)-a-[4-(trifluoromethyl)phenyl]-

OC(c1cccc(c1)C(F)(F)F)c1ccc(cc1)C(F)(F)F Request for Quotation
Chemical Name: Benzenemethanol, 3-(trifluoromethyl)-a-[4-(trifluoromethyl)phenyl]-
CAS Number: 203915-48-4
Product Number: AG002970(AGN-PC-0QU2Y4)
Synonyms:
MDL No:
Molecular Formula: C15H10F6O
Molecular Weight: 320.2297

Identification/Properties

Properties
MP:
48-50℃
Form:
Solid
Computed Properties
Molecular Weight:
320.234g/mol
XLogP3:
4.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
2
Exact Mass:
320.064g/mol
Monoisotopic Mass:
320.064g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
356
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (3-(Trifluoromethyl)phenyl)(4-(trifluoromethyl)phenyl)methanol, also known as $name$, is a versatile chemical reagent commonly used in organic synthesis. Its unique structure containing trifluoromethyl groups makes it valuable for introducing fluorine atoms into organic molecules, a process known as fluorination. $name$ is particularly useful in the preparation of pharmaceuticals, agrochemicals, and materials science. Its presence can enhance the bioavailability, potency, and metabolic stability of drug candidates, making it an essential building block in drug discovery and development. In addition, $name$ can be utilized in the synthesis of specialty chemicals, such as pesticides and advanced materials, where the introduction of fluorine-containing moieties is desired for specific properties. Overall, the application of (3-(Trifluoromethyl)phenyl)(4-(trifluoromethyl)phenyl)methanol in chemical synthesis lies in its ability to facilitate the efficient and controlled introduction of trifluoromethyl groups into organic molecules, enabling the creation of diverse and valuable compounds for various industries.