58285-74-8

Upstream product

• 823-86-9 N-(4-chlorophenyl)hydroxylamine 
• 106-47-8 4-chloro-aniline 
• 121-33-5 vanillin 
• 52010-26-1 C₁₄H₁₂ClNO₃ 

Downstream Products

• 65729-43-3 4-[3,4-bis-(4-chloro-phenyl)-4,5-dihydro-[1,2,4]oxadiazol-5-yl]-2-methoxy-phenol 
• 51264-93-8 (4-{[(E)-4-Chloro-phenylimino]-methyl}-2-methoxy-phenoxy)-acetic acid ethyl ester 
• 78721-40-1 (4-{[(E)-4-Chloro-phenylimino]-methyl}-2-methoxy-phenoxy)-acetic acid hydrazide 
• 78721-42-3 C₂₃H₂₁ClN₄O₃S 
• 78721-44-5 C₂₄H₂₃ClN₄O₃S 
• 78721-43-4 C₂₄H₂₃ClN₄O₃S 
• 78721-45-6 C₂₃H₂₀Cl₂N₄O₃S 
• 78721-46-7 C₂₅H₂₅ClN₄O₄S 
• 354786-65-5 4-(di(1H-indol-3-yl)methyl)-2-methoxyphenol 
• 121-34-6 3-methoxy-4-hydroxybenzoic acid 
• 1602-00-2 bis-(4-chloro-phenyl)-diazene 
• 1401205-00-2 C₂₁H₁₉ClN₂O₃ 
• 58285-81-7 4-(4-chloroanilinomethyl)-2-methoxyphenol 
• 1401205-11-5 C₂₁H₁₉ClN₂O₂S 

Relevant academic research and scientific papers

Synthesis and biological evaluation of novel N, N′-disubstituted urea and thiourea derivatives as potential anti-melanoma agents

Two series of urea and thiourea derivatives (1a11a, 1b11b) have been synthesized; all the 22 compounds were reported for the first time. Their anti-proliferative activities against the melanoma cell line B16-F10 were evaluated. Among the compounds tested,

GREEN SYNTHESIS OF ARYL ALDIMINES USING ETHYL LACTATE

The present invention relates to a method for preparing aryl aldimines. In particular, the present invention relates to methods of preparing aryl aldimines that uses environmentally friendly solvent systems.

Synthesis and voltammetric behaviour of some biologically active imines

A series of 4-{[(4-phenyl)imino}methyl}-2-methoxyphenols were synthesized and the chemical structure of these compounds were confirmed by elemental and spectral analysis. The voltammetric behaviour of all synthesized compounds was studied on DME and HMDE

Magnesium perchlorate as an efficient catalyst for the synthesis of imines and phenylhydrazones

Magnesium perchlorate has been found to be an efficient catalyst for the synthesis of imines and phenylhydrazones by the reaction of carbonyl compounds with amines and phenylhydrazine in high yields at room temperatures and in short times. The condensation of less electrophilic carbonyl compounds with poorly nucleophilic amines affords the imines in excellent yields.

Synthesis and Reduction of Nitrones of Vanillin

Four new vanillin nitrones have been synthesized by condensing vanillin with various arylhydroxylamines.Reduction with sodium borohydride and deoxygenation with zinc dust and acetic acid were studied.

Some New Schiffs Bases Derived from Vanillin as Possible Anticonvulsants

Twenty new anilino- benzylidenes a ten anilino-methyleneoxy>benzylidenes were synthesised.Seven of these compounds when screened for anticonvulsav-activity aga