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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)-

Benzeneethanol, 2,4,5-trifluoro-

OCCc1cc(F)c(cc1F)F Request for Quotation
Chemical Name: Benzeneethanol, 2,4,5-trifluoro-
CAS Number: 883267-70-7
Product Number: AG0047DR(AGN-PC-01LRHL)
Synonyms:
MDL No:
Molecular Formula: C8H7F3O
Molecular Weight: 176.1358

Identification/Properties

Properties
BP:
205.3°C at 760 mmHg
Form:
Solid
Refractive Index:
1.4732
Computed Properties
Molecular Weight:
176.138g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
176.045g/mol
Monoisotopic Mass:
176.045g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
142
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#:
N/A
Hazard Statements:
H302-H315-H320-H335
Precautionary Statements:
P264-P270-P301+P312-P330
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(2,4,5-Trifluorophenyl)ethanol is a versatile compound widely used in chemical synthesis due to its unique properties. Specifically, this compound serves as a valuable building block in the synthesis of various pharmaceuticals, agrochemicals, and materials. Its trifluorinated phenyl group provides enhanced reactivity and stability, making it a valuable intermediate in organic transformations.In chemical synthesis, 2-(2,4,5-Trifluorophenyl)ethanol can be utilized as a key starting material for the preparation of diverse organic compounds. The trifluorinated phenyl group can undergo various functionalization reactions, such as halogenation, substitution, and coupling reactions, enabling the synthesis of complex molecules with precise control over regioselectivity and stereochemistry.Moreover, the hydroxyl group in 2-(2,4,5-Trifluorophenyl)ethanol can participate in versatile chemical transformations, including oxidation, esterification, and ether formation. This functional group offers opportunities for further derivatization to modulate the compound's properties and tailor its reactivity for specific synthetic applications.Overall, 2-(2,4,5-Trifluorophenyl)ethanol plays a crucial role in chemical synthesis by serving as a valuable intermediate with a trifluorinated phenyl moiety, enabling the preparation of diverse organic compounds with enhanced reactivity and functionality.