N-fluorobenzenesulfonamide

Modify Date: 2024-01-02 19:02:56

N-fluorobenzenesulfonamide Structure
N-fluorobenzenesulfonamide structure
Common Name N-fluorobenzenesulfonamide
CAS Number 133745-75-2 Molecular Weight 315.341
Density 1.5±0.1 g/cm3 Boiling Point 471.4±28.0 °C at 760 mmHg
Molecular Formula C12H10FNO4S2 Melting Point 114-116 °C
MSDS Chinese USA Flash Point 238.9±24.0 °C
Symbol GHS07
GHS07
Signal Word Warning

 Names

Name N-Fluorobenzenesulfonimide
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.5±0.1 g/cm3
Boiling Point 471.4±28.0 °C at 760 mmHg
Melting Point 114-116 °C
Molecular Formula C12H10FNO4S2
Molecular Weight 315.341
Flash Point 238.9±24.0 °C
Exact Mass 315.003540
PSA 88.28000
LogP 2.65
Vapour Pressure 0.0±1.2 mmHg at 25°C
Index of Refraction 1.600

 Safety Information

Symbol GHS07
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 26-37/39
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2935009090

 Synthetic Route

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N-fluorobenzenesulfonamide Structure

N-fluorobenzene...

CAS#:133745-75-2

Literature: Tetrahedron, , vol. 69, # 24 p. 4933 - 4937

 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%

 Articles5

More Articles
Enantioselective fluorination of tert-butoxycarbonyl lactones and lactams catalyzed by chiral Pd(II)-bisphosphine complexes.

J. Org. Chem. 72 , 246, (2007)

An efficient catalytic enantioselective fluorination of tert-butoxycarbonyl lactones and lactams is reported. Reactions of the lactone substrates proceeded smoothly in an alcoholic solvent with a cata...

Statistical limits to the identification of ion channel domains by sequence similarity.

J. Fluor. Chem. 127 , 755, (2006)

The study of ion channel function is constrained by the availability of structures for only a small number of channels. A commonly used bioinformatics technique is to assert, based on sequence similar...

Development of GSKDevelopment of GSK's reagent guides – embedding sustainability into reagent selections reagent guides – embedding sustainability into reagent selection. Adams JP, et al.

Green Chem. 15 , 1542-1549 , (2013)

 Synonyms

WSR&NFSWR
Benzenesulfonamide, N-fluoro-N-(phenylsulfonyl)-
Fluorodi(phenylsulfonyl)amine
N-Fluoro-N-(phenylsulfonyl)benzenesulfonamide
N-(benzenesulfonyl)-N-fluorobenzenesulfonamide
N-Fluorobis(phenylsulfonyl)amine
N-Fluorodi(benzenesulfonyl)amine,N-Fluorodibenzenesulfonimide,NFSI
NFSI
N-Fluorodi(benzenesulfonyl)amine
MFCD00144885
N-fluorobenzenesulfonamide
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