TRIFLUOROMETHANESULFONAMIDE

Modify Date: 2025-08-25 17:49:42

TRIFLUOROMETHANESULFONAMIDE Structure
TRIFLUOROMETHANESULFONAMIDE structure
Common Name TRIFLUOROMETHANESULFONAMIDE
CAS Number 421-85-2 Molecular Weight 149.09200
Density 1.73g/cm3 Boiling Point 164.6ºC at 760 mmHg
Molecular Formula CH2F3NO2S Melting Point 120-124 °C(lit.)
MSDS Chinese USA Flash Point 53.3ºC
Symbol GHS07
GHS07
Signal Word Warning

 Names

Name trifluoromethanesulfonamide
Synonym More Synonyms

 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

 Safety Information

Symbol GHS07
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

 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%

 Articles3

More 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...

 Synonyms

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
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