79795-85-0

Upstream product

• 121-33-5 vanillin 
• 57-11-4 stearic acid 
• 112-76-5 Stearoyl chloride 

Downstream Products

• 1086052-42-7 C₃₂H₄₈N₂O₃ 
• 1159214-64-8 C₅₈H₈₈N₂O₆ 
• 1124126-07-3 C₃₂H₄₇NO₃ 
• 1211396-28-9 2-methoxy-4-[(E)-4-phenoxyphenyliminomethyl]phenyl octadecanoate 
• 1236308-50-1 methyl (E,S)-3-methyl-2-(3-methoxy-4-stearoyloxybenzylideneamino)-butyrate 
• 1412860-21-9 C₂₉H₄₈O₅ 
• 1417183-32-4 C₃₄H₅₁NO₄*ClH 
• 1417182-44-5 C₃₄H₅₁NO₄ 
• 1314034-88-2 5-methyl-2-(3-methoxy-4-stearoyloxyphenyl)-1H-benzimidazole 
• 1198406-33-5 C₃₈H₅₁NO₃ 
• 1254182-12-1 C₅₆H₇₈N₂O₇ 
• 1289424-26-5 methyl (E,S)-2-(3-methoxy-4-stearoyloxybenzylideneamino)-3-phenylpropionate 
• 1138818-19-5 C₃₂H₅₃NO₃ 

Relevant academic research and scientific papers

Esters derived from vanillin and vanillal and aromatic and functionalized aliphatic carboxylic acids

Reactions of vanillin and vanillal with aromatic and functionally substituted aliphatic carboxylic acid chlorides in the presence of pyridine afforded the corresponding previously unknown esters.

A facile, versatile procedure for the preparation of fatty acid esters suitable for glc or hplc analyses

The preparation of fatty acid methyl esters for glc analyses and of various aryl esters for hplc analyses has traditionally been carried out in totally unrelated operations.This paper draws attention to the use of fatty acid-trifluoroacetic acid mixed anhydrides which may be directly and efficiently converted into either type of esters.The utility of the method was demonstrated by the preparation of series of methyl, 2-naphthyl, and vanillin fatty acid esters.The spectral characterization of some aryl fatty acid esters is recorded.