52326-08-6

Basic information

• Product Name: Benzenamine, 4-fluoro-N-sulfinyl-
• CAS NO: 52326-08-6
• Molecular Formula: C6H4FNOS
• Molecular Weight: 157.168
• Mol File: 52326-08-6.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzenamine, 4-fluoro-N-sulfinyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 4-fluoro-N-sulfinyl-(52326-08-6)
• EPA Substance Registry System: Benzenamine, 4-fluoro-N-sulfinyl-(52326-08-6)

Safety Data

• Hazardous Substances Data: 52326-08-6(Hazardous Substances Data)

Upstream product

• 371-40-4 4-fluoroaniline 

Downstream Products

• 6633-22-3 N-(4-fluorophenyl)maleimide 
• 181651-02-5 N-(4-fluorophenyl)ethenesulfinamide 
• 81720-50-5 5-p-fluorophenyl-2,4,6-trimethylcyclo-1,3-dioxa-5-aza-2,4,6-triborane 
• 1520119-65-6 N-(4-fluorophenyl)butane-2-sulfinamide 
• 1520120-46-0 2-(4-fluorophenyl)-1-oxo-1-sec-butyl-1λ⁶-thia-2,6-diazacyclohex-6-en-3-one 
• 1520120-17-5 3-{[(4-fluoroanilino)oxo-sec-butyl-1λ⁶-sulfanylidene]amino}propanoic acid 
• 1520119-89-4 ethyl 3-{[(4-fluoroanilino)oxo-sec-butyl-1λ⁶-sulfanylidene]amino}propanoate 
• 1344680-03-0 (R)-N-(4-fluorophenyl)-2-mercapto-2-phenylbutanamide 
• 1344679-92-0 (1R,4S)-N-(4-fluorophenyl)-4-ethyl-4-phenyl-1,2-thiazetidin-3-one 1-oxide 
• 1344680-08-5 (1S,4R)-N-(4-fluorophenyl)-4-ethyl-4-phenyl-1,2-thiazetidin-3-one 1-oxide 
• 84790-08-9 3,5-di-p-fluorophenyl-2,4,6-trimethyl-cyclo-1-oxa-3,5-diaza-2,4,6-triborane 
• 13463-40-6 iron pentacarbonyl 
• 14741-34-5 tricarbonyl bis(triphenylphosphine) iron 
• 35679-07-3 tetracarbonyl(triphenylphosphine)iron 

Relevant articles and documents

Synthesis of benzothiazine sulfonamides via heteroatomic Diels-Alder reaction of para-fluoro-N-sulfinylaniline with bicyclo[2.2.1]heptenes

Reaction of 4-fluoro-N-sulfinylaniline with norbornene and norbornadiene has afforded the Diels-Alder adducts of benzothiazine structure that have been oxidized into the corresponding benzothiazine sulfonamides. Structure of the obtained compounds and ste

Synthesis of six-membered cyclic sulfonimidamides

A general synthetic route to six-membered cyclic N-aryl- and N-alkyl-substituted sulfonimidamides via an intramolecular ring closure of suitably functionalised acyclic sulfonimidamides is described. The structure of this new ring system was confirmed by v

Substituted N-aryl alk-1-enesulfinamides: Preparation, properties and conversion into the corresponding indole compounds [1]

Reaction of vinylic organometallic derivatives with N-sulfinyl arenamines 2 affords the title sulfinamides 3. On heating their solutions in selected solvents to 80-124 °C, these sulfinamides are converted into the corresponding indoles 6, probably via a [3.3]-sigmatropic rearrangement to intermediates VIII which undergo an intramolecular carbophilic reaction of the nitrogen atom with the neighboring sulfine group, followed by elimination of HSOH. The triethyloxonium tetrafluoroborate- or boron trifluoride etherate catalyzed conversion 3 → 6 can be carried out at a much lower temperature. Elsevier,.