(3,5-Bis(trifluoromethyl)phenyl)methanol

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Names

[ CAS No. ]:
32707-89-4

[ Name ]:
(3,5-Bis(trifluoromethyl)phenyl)methanol

[Synonym ]:
EINECS 251-168-9
Benzenemethanol, 3,5-bis(trifluoromethyl)-
[3,5-Bis(trifluoromethyl)phenyl]methanol
[3,5-Di(trifluoromethyl)phenyl]methanol
3,5-Bis(trifluoromethyl)benzenemethanol
3,5-Bis(Trifluoromethyl)benzyl alcohol
[3,5-Bis(trifluoromethyl)phenyl]methan-1-ol
3,5-Di(trifluoromethyl)benzyl alcohol
FXFFR C1Q EXFFF
MFCD00009907
(3,5-Bis(trifluoromethyl)phenyl)methanol

Chemical & Physical Properties

[ Density]:
1.4±0.1 g/cm3

[ Boiling Point ]:
173.9±35.0 °C at 760 mmHg

[ Melting Point ]:
53-56 °C(lit.)

[ Molecular Formula ]:
C9H6F6O

[ Molecular Weight ]:
244.134

[ Flash Point ]:
97.8±0.0 °C

[ Exact Mass ]:
244.032288

[ PSA ]:
20.23000

[ LogP ]:
2.46

[ Vapour Pressure ]:
0.8±0.3 mmHg at 25°C

[ Index of Refraction ]:
1.415

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-S37/39-S36/37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2906299090

Synthetic Route

Precursor & DownStream

Precursor

  • 3,5-Bis(trifluoromethyl)benzaldehyde
  • 3,5-Bis(trifluoromethyl)benzoic acid
  • Formaldehyde
  • (3 5 bis(trifluoromethyl)phenyl)magnesi&

DownStream

  • 3,5-Bis(Trifluoromethyl)benzyl bromide
  • 3,5-Bis(trifluoromethyl)benzaldehyde
  • 3,5-BIS(TRIFLUOROMETHYL)BENZYL METHANESULPHONATE
  • 3,5-Bis(trifluoromethyl)benzyl chloride
  • 2-[[3,5-bis(trifluoromethyl)phenyl]methoxy]-1-phenylethanone
  • 1-Methyl-3,5-bis(trifluoromethyl)benzene

Customs

[ HS Code ]: 2906299090

[ Summary ]:
2906299090 other aromatic alcohols。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0%

Articles

Amide-based atropisomers in tachykinin NK1-receptor antagonists: synthesis and antagonistic activity of axially chiral N-benzylcarboxamide derivatives of 2,3,4,5-tetrahydro-6H-pyrido [2, 3-b][1,5] oxazocin-6-one. Ishichi Y, et al.

Tetrahedron 60(20) , 4481-90, (2004)


More Articles


Related Compounds

  • (3,5-bis(trifluoromethyl)phenyl)(p-tolyl)methanol
  • (3,5-Bis-trifluoromethyl-phenyl)-(4-fluoro-phenyl)-methanol
  • (3,5-Bis-trifluoromethyl-phenyl)-(2,3-dihydro-benzofuran-5-yl)-methanol
  • [3,5-bis(trifluoromethyl)phenyl]-[3-(3,4-dichlorophenyl)piperazin-1-yl]methanone
  • [3,5-Bis(trifluoromethyl)phenyl]acetic acid
  • (3 5 bis(trifluoromethyl)phenyl)magnesi&
  • NaPropylaNa[2a(2a{2a[2a(Napropyl-perfluorooctanesulfonamido)ethoxy]ethoxy}ethoxy)ethyl]perfluorooctanea1asulfonamide
  • Potassium N-methyl(perfluorohexanesulfonamido)acetate
  • 3-[[(Perfluorooctyl)sulfonyl]methylamino]-N,N,N-trimethylpropanaminium iodide
  • Sodium 2-[[3-[(perfluorodecyl)ethylthio]-1-oxopropyl]amino]-2-methyl-1-propanesulfonate
  • Hexadecafluoro-1,4-piperazinediethanesulfinic acid sodium salt (1:2)
  • Triethylammonium perfluoroheptane sulfonate
  • 3-[[(Perfluorohexyl)sulfonyl]-N-methylamino]-N,N,N-trimethyl-1-propanaminium iodide (1:1)
  • 2-(4-Trimethylammoniophenyl)perfluoro(4-methyl-3-(propan-2-yl)pent-2-ene) iodide
  • 4-[(Perfluorononyl)oxy]benzenesulfonic acid ammonium salt
  • N,N,N-Trimethyl-2-[2-methyl-1-oxo-3-[(perfluoroheptyl)ethylthio]propoxy]ethanaminium iodide (1:1)
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