134898-18-3

Upstream product

• 28867-76-7 benzaldehyde benzylidenehydrazone 
• 588-68-1 1,2-di(benzylidene)hydrazine 

Downstream Products

• 1015074-02-8 C₂₀H₂₂N₄O₈S₂ 
• 1015074-06-2 C₂₆H₃₄N₄O₈S₂ 
• 134898-03-6 C₃₀H₂₆N₈O₁₀S₂ 
• 134898-02-5 C₂₂H₂₈N₆O₆S₂ 
• 134897-98-6 C₂₀H₂₄N₆O₄S₂ 
• 1015074-10-8 C₂₈H₃₈N₄O₈S₂ 
• 1015074-08-4 C₂₂H₂₆N₄O₈S₂ 
• 134897-95-3 N,N'-Bis-[1-[3-(3,5-dimethyl-morpholine-4-sulfonyl)-phenyl]-meth-(E)-ylidene]-hydrazine 
• 134897-97-5 C₁₄H₁₆N₆O₄S₂ 

Relevant academic research and scientific papers

A comparative study on some diaryl azines amino acid derivatives

Benzaldehydeazines, p-anisaldehydeazines, and thiophene-2-carboxaldehyde azines react with excess chlorosulfonic acid to give corresponding disulfonyl chlorides 1,13, and 24. These were condensed with nucleophiles to give disulfonyl amino acid derivatives

CHLOROSULFONATION OF DIARYL AZINES

Benzaldehyde- and o-, m-, p-anisaldehyde azines; thiophene-2-carboxaldehyde, and biphenyl-4-carboxaldehyde azines (1-8) reacted with excess chlorosulfonic acid to give the disulphonyl chlorides (1a-8a).These were condensed with amines and hydrazine to give 27 derivatives, (Table I) for biocidal evaluation.The orientation of sulfonation is discussed in relation to the stereoelectronic factors and the spectral data.Attempted chlorosulfonation of furan-2-carboxaldehyde azine (9) gave an impure product which could not be clearly characterized as the morpholidate derivative.