765298-70-2

Upstream product

• 121-33-5 vanillin 
• 111-64-8 n-octanoic acid chloride 
• 124-07-2 Octanoic acid 

Downstream Products

• 1086052-39-2 C₂₂H₂₈N₂O₃ 
• 1159214-61-5 C₃₈H₄₈N₂O₆ 
• 1124126-04-0 C₂₂H₂₇NO₃ 
• 956294-13-6 C₂₅H₂₆O₅ 
• 1138818-14-0 C₂₂H₃₃NO₃ 
• 1236308-48-7 methyl (E,S)-2-(4-capryloyloxy-3-methoxybenzylideneamino)-3-methylbutyrate 
• 1254182-10-9 C₄₆H₅₈N₂O₇ 
• 1198407-12-3 C₂₈H₃₃NO₃ 
• 1198406-29-9 C₂₈H₃₁NO₃ 
• 1211396-25-6 2-methoxy-4-[(E)-4-phenoxyphenyliminomethyl]phenyl octanoate 

Relevant academic research and scientific papers

Vanillin esters in reactions with indan-1,3-dione

2-Methoxy-4-(12-oxo-12H-benzo[f]indeno[1,2-b]quinolin-13-yl)phenyl esters of carboxylic acids were synthesized by the three component condensation of indan-1,3-dione, 2-naphthylamine, and O-acylvanillin. 2-Arylidenindan-1,3-diones formed during the reaction were isolated. Springer Science+Business Media, Inc. 2006.

Preparative synthesis of vanillin and vanillal alkanoates

Procedures for preparing vanillin and vanillal alkanoates were developed.

Vanillin esters of aliphatic acids in the synthesis of 4,7-phenanthroline derivatives

Condensation of vanillin esters of aliphatic acids with 6-aminoquinoline and cyclic c-diketones (1,3-cyclohexanedione and dimedone) afforded new 2-methoxy-4-(11-oxo-7,8,9,10,11,12-hexahydrobenzo[b][4,7]phenanthrolin-12-yl) phenyl esters of carboxylic acids.

Reaction of long-chain vanillyl esters with ch-acids and 2-naphthylamine

The previously unknown4-(alkyl-11-oxo-7,8,9,10,11,12-hexahydrobenzo[a] acridin-12-yl)-and4-(alkyl-1,8-dioxo-2,3,4,5,6,7,8,9-octahydro-1H-xanthen-9-yl) -2-methoxyphenyl esters of aliphatic (C5-C7, C 12) carboxylic acids were synthesizedvia cascade heterocyclization of cyclohexane-1,3-dione and dimedone with 2-naphthylamine and long-chain vanillyl esters.