844634-13-5

Upstream product

• 121-33-5 vanillin 
• 141-75-3 butyryl chloride 
• 106-31-0 butanoic acid anhydride 

Downstream Products

• 1086052-37-0 C₁₈H₂₀N₂O₃ 
• 1159214-59-1 C₃₀H₃₂N₂O₆ 
• 1124126-02-8 C₁₈H₁₉NO₃ 
• 452363-05-2 C₂₁H₁₈O₅ 
• 1138818-08-2 C₁₈H₂₅NO₃ 
• 1211396-23-4 2-methoxy-4-[(E)-4-phenoxyphenyliminomethyl]phenyl butanoate 
• 1289424-17-4 methyl (E,S)-2-(4-butyryloxy-3-methoxybenzylideneamino)-3-phenylpropionate 
• 1198407-06-5 C₂₄H₂₅NO₃ 

Relevant academic research and scientific papers

Newly designed and synthesized curcumin analogs with in vitro cytotoxicity and tubulin polymerization activity

Novel curcumin analogs with 4-piperidone ring were designed, synthesized, and evaluated for their cytotoxic activities against five different cancer cell lines. 3,5-bis(4-Hydroxy-3-methoxybenzylidene)-4-oxo-N-phenylpiperidine-1-carbothioamide (XIIe) exhib

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.

Vanilline alkanoates in the synthesis of hexahydrobenzacridine and octahydroxanthene derivatives

Cascade heterocyclization of 1,3-cyclohexanedione and dimedone with 2-naphthylamine and vanilline esters gave derivatives of 2-methoxy-4-(alkyl-11- oxo-7,8,9,10,11,12-hexahydrobenz[a]acridin-12-yl)- and 2-methoxy-4-(alkyl-1,8- dioxo-2,3,4,5,6,7,8,9-octahydro-1H-xanthen-9-yl)phenyl esters of aliphatic (C1- C4 ) carboxylic acids. 2005 Pleiades Publishing, Inc.

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.