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4-Trifluoromethylphenol

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Products Intro: Product Name:4-(Trifluoromethyl)phenol
CAS:402-45-9
Purity:98% (Min,GC) Package:1G;1KG;100KG
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Products Intro: Product Name:4-(Trifluoromethyl)phenol
CAS:402-45-9
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CAS:402-45-9
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Products Intro: Product Name:4-(trifluoromethyl)phenol;p-Trifluoromethylphenyl;4-Trifluoromethylphenol;4-Hydroxybenzotrifluoride
CAS:402-56-9
Purity:98% Package:1KG;25KG

4-Trifluoromethylphenol manufacturers

4-Trifluoromethylphenol Basic information
Preparation method Chemical Characteristics Uses
Product Name:4-Trifluoromethylphenol
Synonyms:alpha,alpha,alpha-Trifluoro-p-cresol,loosecrystals;Phenol, 4-(trifluoromethyl)-;P-HYDROXYBENZOTRIFLUORIDE;P-(TRIFLUOROMETHYL)PHENOL;ALPHA,ALPHA,ALPHA-TRIFLUORO-4-CRESOL;ALPHA,ALPHA,ALPHA-TRIFLUORO-P-CRESOL;4-HYDROXYBENZOTRIFLUORIDE;4-HYDROXY-ALPHA,ALPHA,ALPHA-TRIFLUOROTOLUENE
CAS:402-45-9
MF:C7H5F3O
MW:162.11
EINECS:206-945-7
Product Categories:Fluorochemicals;Trifluoromethylbenzene serise;Aromatic Phenols;Phenol&Thiophenol&Mercaptan;bc0001
Mol File:402-45-9.mol
4-Trifluoromethylphenol Structure
4-Trifluoromethylphenol Chemical Properties
Melting point 45-47 °C(lit.)
Boiling point 71.5-72 °C (8 mmHg)
density 1.3226 (estimate)
Fp 183 °F
storage temp. Store at <= 20°C.
Water Solubility Insoluble in water
solubility Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
pkapK1:8.675 (25°C)
form Crystals
color White to yellow-brown
BRN 1637019
Stability:Light Sensitive
InChIKeyBAYGVMXZJBFEMB-UHFFFAOYSA-N
CAS DataBase Reference402-45-9(CAS DataBase Reference)
NIST Chemistry Referencep-Hydroxybenzotrifluoride(402-45-9)
EPA Substance Registry System4-(Trifluoromethyl)phenol (402-45-9)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 22-37/38-41-36/37/38
Safety Statements 26-39-24/25
RIDADR UN 2926 4.1/PG 2
WGK Germany 3
Hazard Note Irritant/Keep Cold
PackingGroup 
HS Code 29081000
MSDS Information
ProviderLanguage
alpha,alpha,alpha-Trifluoro-p-cresol English
SigmaAldrich English
ACROS English
ALFA English
4-Trifluoromethylphenol Usage And Synthesis
Preparation methodChlorosilane and bromotrifluoromethane at-59℃form trifluoromethylsilane. Trifluoromethylsilane and benzoquinone in the presence of catalyst form 4-triethylsiloxy-4-trifluoromethyl-2,5-cyclohexadien-1-ketone which is reduced by zinc powder to p-trifluoromethylphenol with a yield of 71%. This method avoids the use of  hydrofluoric acid in the traditional process but  should be carried out under anhydrous conditions.If there were water trifluoromethyl silane would rapidly become silanol under the effect of water and alkali. The catalyst used in the reaction is alkali of which the strength has nothing to do with the catalytic activity. By now the role of catalyst is still unknown but the reaction can not proceed without catalyst.
Chemical CharacteristicsOff-white crystal
UsesFor intermediate of medicine and pesticide.
Chemical PropertiesWhite to yellowish-brown crystals
Uses4-(Trifluoromethyl)phenol (4-hydroxybenzotrifluoride) was used in the synthesis of diaryl ether.
UsesIntermediates of Liquid Crystals
DefinitionChEBI: 4-(trifluoromethyl)phenol is a member of the class of (trifluoromethyl)benzenes that is p-cresol in which the methyl group is perfluorinated. It is a metabolite of the drug fluoxetine. It has a role as a marine xenobiotic metabolite and a drug metabolite. It is a member of phenols and a member of (trifluoromethyl)benzenes. It is functionally related to a (trifluoromethyl)benzene and a p-cresol.
Synthesis Reference(s)The Journal of Organic Chemistry, 54, p. 2873, 1989 DOI: 10.1021/jo00273a020
General Description4-(Trifluoromethyl)phenol molecule, bound at the active site of H61T (His-61→Thr) mutant, shows strong density.
Tag:4-Trifluoromethylphenol(402-45-9) Related Product Information
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