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TRIFLUOROMETHANESULFONAMIDE

Names

[ CAS No. ]:
421-85-2

[ Name ]:
TRIFLUOROMETHANESULFONAMIDE

[Synonym ]:
trifluoro-methanesulfonic acid amide
1bcd
Trifluoromethylsulfonamide
TrifluoroMethanesulfonaMide
trifluoromethanesulphonamide
TRIFLUOROMETHANE SULFONAMIDE
EINECS 431-270-1
Methanesulfonamide,1,1,1-trifluoro
triflylamine
Triflamide
1,1,1-trifluoromethanesulfonamide
trifluoromethyl-sulphonamide
MFCD00068714

Chemical & Physical Properties

[ Density]:
1.73g/cm3

[ Boiling Point ]:
164.6ºC at 760 mmHg

[ Melting Point ]:
120-124 °C(lit.)

[ Molecular Formula ]:
CH2F3NO2S

[ Molecular Weight ]:
149.09200

[ Flash Point ]:
53.3ºC

[ Exact Mass ]:
148.97600

[ PSA ]:
68.54000

[ LogP ]:
1.57580

[ Vapour Pressure ]:
1.95mmHg at 25°C

[ Index of Refraction ]:
1.369

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H315-H319-H335

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

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

[ Hazard Codes ]:
Xn: Harmful;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2935009090

Precursor & DownStream

Customs

[ HS Code ]: 2935009090

[ Summary ]:
2935009090 other sulphonamides VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:35.0%

Articles

Intrinsic thermodynamics of ethoxzolamide inhibitor binding to human carbonic anhydrase XIII.

BMC Biophys. 5 , 12, (2013)

Human carbonic anhydrases (CAs) play crucial role in various physiological processes including carbon dioxide and hydrocarbon transport, acid homeostasis, biosynthetic reactions, and various pathologi...

Role of hepatic carbonic anhydrase in de novo lipogenesis.

Biochem. J. 310 ( Pt 1) , 197-202, (1995)

The role of carbonic anhydrase in de novo lipid synthesis was examined by measuring [1-14C]acetate incorporation into total lipids, fatty acids and non-saponifiable lipids in freshly isolated rat hepa...

Synthesis of N-[2-(2,4-Difluorophenoxy)trifluoromethyl-3-pyridyl]sulfonamides and their inhibitory activities against secretory phospholipase A₂.

Chem. Pharm. Bull. 59(8) , 1069-72, (2011)

N-[2-(2,4-Difluorophenoxy)trifluoromethyl-3-pyridyl]sulfonamide derivatives 3-6 were prepared by the reaction of 3-pyridylamines and sulfonyl chlorides. Inhibitory activities of these compounds toward...


More Articles


Related Compounds