4-[(Trifluoromethyl)sulfanyl]phenol

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Names

[ CAS No. ]:
461-84-7

[ Name ]:
4-[(Trifluoromethyl)sulfanyl]phenol

[Synonym ]:
Phenol, 4-[(trifluoromethyl)thio]-
4-(TrifluoroMethylthio)phenol
4-((Trifluoromethyl)thio)phenol
MFCD00036035
4-[(Trifluoromethyl)thio]phenol
4-(trifluoromethylsulfanyl)phenol
4-[(Trifluoromethyl)sulfanyl]phenol
QR DSXFFF

Chemical & Physical Properties

[ Density]:
1.5±0.1 g/cm3

[ Boiling Point ]:
170.4±40.0 °C at 760 mmHg

[ Melting Point ]:
57-60 °C(lit.)

[ Molecular Formula ]:
C7H5F3OS

[ Molecular Weight ]:
194.174

[ Flash Point ]:
56.9±27.3 °C

[ Exact Mass ]:
194.001312

[ PSA ]:
45.53000

[ LogP ]:
2.67

[ Vapour Pressure ]:
1.1±0.3 mmHg at 25°C

[ Index of Refraction ]:
1.529

[ Storage condition ]:
Room temperature.

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2930909090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Bromotrifluoromethane (R 13B1)
  • 4,4'-Disulfanediyldiphenol
  • trifluoromethanesulphenyl chloride
  • Phenol
  • Iodotrifluoromethane
  • 4-Mercaptophenol

DownStream

  • 2-chloro-4-(trifluoromethylsulfanyl)phenol
  • 2-propyl-4-(trifluoromethylsulfanyl)phenol
  • 1-prop-2-enoxy-4-(trifluoromethylsulfanyl)benzene
  • 2-prop-2-enyl-4-(trifluoromethylsulfanyl)phenol
  • 1-(3-iodopropoxy)-2-propyl-4-(trifluoromethylsulfanyl)benzene
  • 2-chloro-1-(3-iodopropoxy)-4-(trifluoromethylsulfanyl)benzene
  • 2-Nitro-4-((trifluoromethyl)thio)phenol
  • 4-Hydroxyphenyl trifluoromethyl sulphone

Customs

[ HS Code ]: 2930909090

[ Summary ]:
2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Acid-promoted direct electrophilic trifluoromethylthiolation of phenols.

Org. Biomol. Chem. 13(10) , 3103-15, (2015)

The electrophilic aromatic ring trifluoromethylthiolation of various substituted phenols was accomplished using PhNHSCF3 (N-trifluoromethylsulfanyl)aniline, (1) in the presence of BF3·Et2O (2) or trif...

Synthesis of Toltrazuril.

Chin. J. Pharm. 37(3) , 145, (2006)

Study on the synthesis of toltrazuril. Jiang Z-L, et al.

Chemical Reagents 28(9) , 518, (2006)


More Articles

Related Compounds

  • 2-Amino-4-[(trifluoromethyl)sulfanyl]phenol
  • 2-Nitro-4-[(trifluoromethyl)sulfanyl]phenol
  • 2-Amino-6-bromo-4-[(trifluoromethyl)sulfanyl]phenol
  • 2-Bromo-6-nitro-4-[(trifluoromethyl)sulfanyl]phenol
  • {4-[(Trifluoromethyl)sulfanyl]phenyl}acetic acid
  • {4-[(Trifluoromethyl)sulfanyl]phenyl}acetonitrile
  • 1h-Indazole,1-(2-azidopropyl)-7-bromo-6-methoxy-
  • Methyl 6,9,12,15,18-heneicosapentaenoate
  • (2S,10R)-2-Hydroxynonadecan-10-YL naphthalene-2-carboxylate
  • 1-(5-Bromo-1-methyl-1H-imidazol-2-yl)ethanone
  • N-Boc-5-iodo-DL-norvaline tert-butyl ester
  • Methyl 3-(bromomethyl)oxirane-2-carboxylate
  • N,5-dimethyl-N-(piperidin-3-yl)pyridin-2-amine hydrochloride
  • 1-[(2-chloro-4-fluorophenyl)methyl]-1H-pyrrole-2-carboxylic acid
  • 1-Bromo-3-ethenylcyclopentane
  • (E)-N-(2-(3-methylisoxazol-5-yl)ethyl)but-2-enamide
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