26516-62-1

Upstream product

• 106-40-1 4-bromo-aniline 

Downstream Products

• 5044-47-3 2-(4-bromo-phenyl)-4,5-dimethyl-3,6-dihydro-2H-[1,2]thiazine 1-oxide 
• 395641-81-3 C₉H₁₃BrN₂SSi 
• 13463-40-6 iron pentacarbonyl 
• 52500-74-0 tricarbonyl bis(tri-p-tolylphosphine) iron 
• 52278-75-8 (CO)4FeP(C₆H₄CH₃-p)3 
• 85134-89-0 [Fe(P(4-MeC₆H₄)3)2(CO)2(4-BrC₆H₄NSO)] 
• 182273-77-4 1,1’-bis[1-(4-bromophenylimino)ethyl]ferrocene 
• 1520120-32-4 2-(4-bromophenyl)-1-ethyl-1-oxo-1λ⁶-thia-2,6-diazacyclohex-6-en-3-one 
• 1520120-03-9 3-{[(4-bromoanilino)ethyloxo-1λ⁶-sulfanylidene]amino}propanoic acid 
• 1520119-77-0 ethyl 3-{[(4-bromoanilino)ethyloxo-1λ⁶-sulfanylidene]amino}propanoate 
• 1520119-53-2 N-(4-bromophenyl)ethanesulfinamide 
• 14741-34-5 tricarbonyl bis(triphenylphosphine) iron 
• 35679-07-3 tetracarbonyl(triphenylphosphine)iron 
• 85134-80-1 [Fe(triphenylphosphine)2(CO)2(4-BrC₆H₄NSO)] 

Relevant academic research and scientific papers

Synthesis of benzo-ortho-thiazines S-oxides by diels-alder reaction of N-sulfinylanilines with norbornadiene

From substituted N-sulfinylanilines acting as dienes in the Diels-Alder reaction with norbornadiene S-oxides of benzo-ortho-thiazines were obtained, which were oxidized into the corresponding S,S-dioxides belonging to the class of hybrid thiazinesulfonami

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,.

6?-Cycloadditions of Aryl and New Heteroaryl N-Sulphinylamines With 2,3-Dimethylbuta-1,3-diene: Synthesis, Kinetics, Substituent Effects, Theoretical Calculations, and Reaction Mechanism

A range of new N-sulphinylamine derivatives of heteroaryl rings, including tetrazoles, oxadiazoles, thiadiazoles, thiazoles, and oxazoles is reported.The influence of the -N=S+-O- group on the n.m.r. spectra of the ring to which it i