27126-29-0

Upstream product

• 4380-38-5 4-(4-methoxy-benzylidenamino)-benzoic acid 
• 61439-58-5 ethyl 4-(4-methoxybenzylamino)benzoate 
• 180330-54-5 water ethanol 
• 150-13-0 4-amino-benzoic acid 
• 105-13-5 4-Methoxybenzyl alcohol 
• 94-09-7 p-aminoethylbenzoate 
• 2746-25-0 p-Methoxybenzyl bromide 
• 123-11-5 4-methoxy-benzaldehyde 
• 887751-39-5 N,N-9-fluorenylmethyloxycarbonyl-(4-methoxybenzyl)-4-aminobenzoic acid 
• 925676-13-7 (4-chlorocarbonyl-phenyl)-(4-methoxy-benzyl)-carbamic acid 9H-fluoren-9-ylmethyl ester 

Downstream Products

• 887751-38-4 N-(4-methoxybenzyl)-4-(4-nitrobenzamido)benzoic acid 
• 19717-14-7 4-(4-Nitrobenzoylamino)-benzoic acid 
• 887751-42-0 4-[(4-amino-benzoyl)-(4-methoxy-benzyl)-amino]-benzoic acid 
• 887751-40-8 N,N-9-fluorenylmethyloxycarbonyl-(4-methoxybenzyl)-4-aminobenzoic acid dimer 
• 887751-39-5 N,N-9-fluorenylmethyloxycarbonyl-(4-methoxybenzyl)-4-aminobenzoic acid 

Relevant academic research and scientific papers

In(OTf)3 catalyzed N-benzylation of amines utilizing benzyl alcohols in water

An In(OTf)3-catalyzed N-benzylation of amines utilizing benzyl alcohols through direct C-O bond activation has been reported. The reaction was performed in water without any base, additive, ligand or inert gas protection to afford the chem-selective mono- or bis-alkylated aromatic amines in good to excellent yields.

Solid-phase synthesis of oligo(p-benzamide) foldamers

A coupling protocol has been developed which allows the synthesis of oligo(p-benzamide)s on solid support. Aromatic carboxylic acids are activated in situ with thionyl chloride and used to acylate secondary aromatic amines. N-p-Methoxy benzyl (PMB) as wel

Potential antiatherosclerotic agents. 2. (Aralkylamino)- and (alkylamino)benzoic acid analogues of cetaben

The syntheses of a series of (aralkylamino)- and (alkylamino)benzoic acids, as well as the corresponding esters and sodium salts, are described. The compounds were evaluated in vivo in rats for serum sterol and triglyceride lowering activity and in vitro

Electroreduction of Some Azomethine Compounds at Copper and Copper Amalgam Cathodes

The electrochemical reducibility of some azomethine compounds derived from aniline, its derivatives, 2-aminopyridine, and 2-aminobenzothiazole and aromatic aldehydes at copper and copper amalgam cathodes in acid medium has been investigated.It is found that reducibility of the compounds increases with increase in hydrogen overvoltage of the cathode and decrease in current density.Furthermore the reducibility of the azomethine compounds possessing non-hetero aromatic amine moiety is higher than that of compounds possessing heteroaromatic amine moiety.

Antilipidemic para-[aryl(alkyl or alkenyl)amino]-benzoic acid derivatives

Novel para-[aryl(alkyl or alkenyl)amino]benzoic acids, esters, pharmaceutically acceptable salts and pharmaceutical compositions thereof and a method of lowering serum lipid levels in mammals therewith.