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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-(trifluoromethyl)-

OCCc1ccccc1C(F)(F)F Request for Quotation
Chemical Name: Benzeneethanol, 2-(trifluoromethyl)-
CAS Number: 94022-96-5
Product Number: AG0032VW(AGN-PC-0JTD1A)
Synonyms:
MDL No:
Molecular Formula: C9H9F3O
Molecular Weight: 190.1624

Identification/Properties

Properties
MP:
−3-−2 °C(lit.)
BP:
185°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Refractive Index:
n20/D 1.47(lit.)
Computed Properties
Molecular Weight:
190.165g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
190.061g/mol
Monoisotopic Mass:
190.061g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
155
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


$Name$ is a versatile chemical compound that plays a crucial role in chemical synthesis. Specifically, 2-(2-(Trifluoromethyl)phenyl)ethanol is commonly utilized as a reagent in organic reactions due to its unique chemical properties. This compound serves as a valuable building block in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Its trifluoromethyl group enhances the compound's reactivity and stability, making it a valuable tool in the creation of complex molecular structures. Additionally, 2-(2-(Trifluoromethyl)phenyl)ethanol can be employed as a chiral auxiliary or a protecting group in synthesis strategies, enabling the selective formation of desired products. In summary, this compound is a key player in modern chemical synthesis, facilitating the efficient and controlled creation of diverse compounds with important industrial applications.