<Suppliers Price>

3-(Trifluoromethyl)benzenesulfonyl chloride

Names

[ CAS No. ]:
777-44-6

[ Name ]:
3-(Trifluoromethyl)benzenesulfonyl chloride

[Synonym ]:
3-(Trifluoromethyl)benzenesulphonyl chloride
WSGR CXFFF
MFCD00014724
Benzenesulfonyl chloride, 3-(trifluoromethyl)-
3-trifluoromethylbenzene-1-sulfonyl chloride
m-trifluoromethylbenzenesulfonyl chloride
3-(Trifluoromethyl)benzenesulfonyl chloride
3-trifluoromethylbenzenesulfochloride

Chemical & Physical Properties

[ Density]:
1.5±0.1 g/cm3

[ Boiling Point ]:
261.1±40.0 °C at 760 mmHg

[ Molecular Formula ]:
C7H4ClF3O2S

[ Molecular Weight ]:
244.619

[ Flash Point ]:
111.7±27.3 °C

[ Exact Mass ]:
243.957260

[ PSA ]:
42.52000

[ LogP ]:
2.89

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.481

[ Storage condition ]:
2~8℃

MSDS

Safety Information

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
C:Corrosive;

[ Risk Phrases ]:
R34

[ Safety Phrases ]:
S26-S36/37/39-S45-S25

[ RIDADR ]:
UN 3265 8/PG 2

[ WGK Germany ]:
3

[ Packaging Group ]:
II

[ Hazard Class ]:
8

[ HS Code ]:
2904909090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2904909090

[ Summary ]:
HS:2904909090 sulphonated, nitrated or nitrosated derivatives of hydrocarbons, whether or not halogenated VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Articles

Polymer supported reagents in synthesis: preparation of bicyclo[2.2.2] octane derivates via Tandem Michael addition reactions and subsequent combinatorial decoration.

J. Comb. Chem. 2 , 104-107, (2000)

Chemistry of aminophenols. Part 2: A general and efficient synthesis of indoles possessing a nitrogen substituent at the C4, C5, C6, and C7 positions. Dai et al.

Tetrahedron Lett. 43 , 7699-7702, (2002)

Preparation of N-(a, ß-unsaturated acyl)-sulfonamides. Katritzky et al.

ARKIVOC 4 , 115-124, (2009)


More Articles


Related Compounds

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.