1. Home
  2. Benzenemethanol,4-fluoro-2-(trifluoromethyl)-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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,4-fluoro-2-(trifluoromethyl)-

OCc1ccc(cc1C(F)(F)F)F Request for Quotation
Chemical Name: Benzenemethanol,4-fluoro-2-(trifluoromethyl)-
CAS Number: 220227-29-2
Product Number: AG003LCY(AGN-PC-0QYKLR)
Synonyms:
MDL No:
Molecular Formula: C8H6F4O
Molecular Weight: 194.1263

Identification/Properties

Properties
MP:
55-57 °C
BP:
189.5°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
194.129g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
194.035g/mol
Monoisotopic Mass:
194.035g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
168
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:
H315-H319-H335
Precautionary Statements:
P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


4-Fluoro-2-(trifluoromethyl)benzyl alcohol is a versatile chemical compound widely utilized in chemical synthesis for its unique properties and applications. In organic chemistry, this compound serves as a valuable building block in the synthesis of various complex molecules. Due to the presence of the fluoro and trifluoromethyl groups, 4-Fluoro-2-(trifluoromethyl)benzyl alcohol is capable of participating in a range of chemical reactions, including nucleophilic substitutions and metal-catalyzed transformations. These functionalities enable its use in the preparation of pharmaceuticals, agrochemicals, and materials with tailored properties. The compound's reactivity and stability make it an essential component in the toolkit of synthetic chemists for creating structurally diverse compounds with specific functionalities.