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3,5-Bis(trifluoromethyl)phenol | CAS:349-58-6
3,5-Bis(trifluoromethyl)phenol
  • Name:3,5-Bis(trifluoromethyl)phenol
  • CAS:349-58-6
  • Synonyms:3,5-Di(trifluoromethyl)phenol
  • Molecular Formula:C8H4F6O
  • Molecular Weight:230.11
  • EINESC:206-488-3

Description

Properties

Melting point 20-21 ºC
Boiling point 97 ºC (50 mmHg)
Density 1.511
Refractive index 1.414-1.416

Safety

Symbol(GHS) Xi
Hazard Codes R36/37/38
SDS/MSDS S26;S37/39

SDS

Source SDS/MSDS Samples
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Synthetic Route
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Articles
Peer-Reviewed Papers
Diffusion-free mediator based miniature biofuel cell anode fabricated on a carbon-MEMS electrode.Gobind S Bisht et al.Langmuir : the ACS journal of surfaces and colloids, 28(39), 14055-14064 (2012-09-06) Analysis of aliphatic amines in air samples by HPLC with electrochemical detection.N A Santagati et al.Journal of pharmaceutical and biomedical analysis, 29(6), 1105-1111 (2002-07-12) Validation of malondialdehyde and 4-hydroxy-2-trans-nonenal measurement in plasma by NICI-GC-MS.S Rauli et al.Journal of biochemistry, 123(5), 918-923 (1998-06-19) Sequential C-N and C-O bond formation in a single pot: synthesis of 2H-benzo[b][1,4]oxazines from 2,5-dihydroxybenzaldehyde and amino acid precursors.Javed Iqbal et al.Organic letters, 14(2), 552-555 (2012-01-06) Liquid chromatographic/electrospray ionization mass spectrometric identification of the oxidation end-products of trans-resveratrol in aqueous solutions.Laurent Camont et al.Rapid communications in mass spectrometry : RCM, 24(5), 634-642 (2010-02-16) Synthesis and in vitro antiproliferative activity of new phenylaminoisoquinolinequinones against cancer cell lines.Virginia Delgado et al.Molecules (Basel, Switzerland), 18(1), 721-734 (2013-01-10) A bioanode based on MWCNT/protein-assisted co-immobilization of glucose oxidase and 2,5-dihydroxybenzaldehyde for glucose fuel cells.Chung-Mu Yu et al.Biosensors & bioelectronics, 25(11), 2515-2521 (2010-05-18) The reductive half-reaction of xanthine oxidase. Reaction with aldehyde substrates and identification of the catalytically labile oxygen.M Xia et al.The Journal of biological chemistry, 274(6), 3323-3330 (1999-01-28)
Remarks

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