N-fluorobenzenesulfonamide

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Names

[ CAS No. ]:
133745-75-2

[ Name ]:
N-fluorobenzenesulfonamide

[Synonym ]:
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

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

MSDS

Safety Information

[ Symbol ]:

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

Precursor & DownStream

Precursor

  • Dibenzenesulfonimide

DownStream

  • 3-Fluoro-2-thiophenecarboxylic acid
  • N-fluorobenzenesulfonamide
  • Benzenesulfonic acid
  • 2'-Fluoropropiophenone
  • 2-Fluorocyclohexanone
  • Benzenesulfonamide,N-methyl-
  • 2'-fluoroacetanilide
  • 1-BENZENESULFONYL-PIPERAZINE
  • Dibenzenesulfonimide

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

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)


More Articles


Related Compounds

  • N-fluorobenzenesulfonamide
  • N-tert-butyl-N-fluorobenzenesulfonamide
  • N-Cyclohexyl 4-fluorobenzenesulfonamide
  • N-Benzyl-4-fluorobenzenesulfonamide
  • N-Cyclopropyl-4-fluorobenzenesulfonamide
  • N-allyl-4-fluorobenzenesulfonamide
  • 1-(Propan-2-yl)-1,2,3,4-tetrahydroquinolin-4-amine
  • 2-[3-(Propan-2-yl)phenyl]propan-1-amine
  • 1-(4-Hydroxy-3,4-dihydroquinolin-1(2h)-yl)-2-methylpropan-1-one
  • 1-(4-Hydroxy-3,4-dihydroquinolin-1(2h)-yl)propan-1-one
  • 4-Quinolinol, 1,2,3,4-tetrahydro-1-(1H-imidazol-5-ylsulfonyl)-
  • 5-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2,3-dimethylbenzoic acid
  • [4-(4-Methylphenyl)thiophen-2-yl]methanamine
  • 4-Chloro-2-(3,5-dichlorophenyl)-5-ethyl-6-methylpyrimidine
  • 4-(Cyclopentylmethoxy)piperidine
  • 3-[(dimethyl-1H-1,2,4-triazol-1-yl)methyl]aniline
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