5462-94-2

Usage

Uses

Used in Organic Synthesis:
(2E,4E,6E,8E,10E)-11-phenylundeca-2,4,6,8,10-pentaenal is used as a key intermediate in organic synthesis for the production of various compounds.
Used in Fragrance Industry:
In the fragrance industry, (2E,4E,6E,8E,10E)-11-phenylundeca-2,4,6,8,10-pentaenal is used as a building block for creating complex and unique scents due to its reactive aldehyde functional group.
Used in Pharmaceutical Industry:
(2E,4E,6E,8E,10E)-11-phenylundeca-2,4,6,8,10-pentaenal is used as a starting material or intermediate in the synthesis of pharmaceuticals, taking advantage of its unique structure and reactivity to produce novel drug candidates.
Used in Fine Chemicals Production:
(2E,4E,6E,8E,10E)-11-phenylundeca-2,4,6,8,10-pentaenal is utilized in the production of fine chemicals, where its specific molecular structure and properties are harnessed for specialized applications.

Upstream product

• 58274-72-9 (2E,6E,8E,10E)-5-Methoxy-11-phenyl-undeca-2,6,8,10-tetraenal 
• 14371-10-9 (E)-3-phenylpropenal 
• 123-73-9 trans-Crotonaldehyde 
• 100-52-7 benzaldehyde 
• 58274-72-9 (2E,6E,8E,10E)-5-Methoxy-11-phenyl-undeca-2,6,8,10-tetraenal 
• 32410-52-9 (2E,4E,6E)-7-phenylhepta-2,4,6-trienal 
• 445398-86-7 (4E,6E)-7-phenyl-4,6-heptadien-1-ol 

Downstream Products

• 123964-81-8 2-((Ξ)-11t-phenyl-undeca-2t,4t,6t,8t,10-pentaenylidene)-benzo[b]thiophen-3-one 
• 113134-63-7 5-(11t-phenyl-undeca-2t,4t,6t,8t,10-pentaenylidene)-barbituric acid 
• 112745-37-6 3-ethyl-5-((1Ξ)-11t-phenyl-undeca-2t,4t,6t,8t,10-pentaenylidene)-2-thioxo-thiazolidin-4-one 
• 121474-86-0 3-(10t-phenyl-deca-1,3t,5t,7t,9-pentaen-t-yl)-benzo[f]quinoline-1-carboxylic acid 
• 91375-69-8 1,13t-diphenyl-trideca-2t,4t,6t,8t,10t,12-hexaen-1-one 
• 84654-96-6 2-cyano-13t-phenyl-trideca-2ξ,4t,6t,8t,10t,12-hexaenoic acid ethyl ester 

Relevant academic research and scientific papers

Stereoselective organocatalytic oxidation of alcohols to enals: A homologation method to prepare polyenes

A novel method for organocatalytic oxidation through oxidative enamine catalysis was developed with excellent compatibility for the direct syntheses of enals from simple saturated alcohols. By using this amine-catalyzed IBX-oxidation, a wide range of aromatic and aliphatic substituted enals were successfully generated in high yields and exclusively stereoselective E-geometry. Moreover, varying the solvents and/or the loading amounts of IBX allowed for the selective oxidation of alcohols and aldehydes. Importantly, the homologous application of this method provided a selective and efficient way of preparing various highly sensitive conjugated polyene frameworks, which are enriched in natural products.

ω-Halogeno polyenals: Preparation and application to a one-pot synthesis of polyenals from carbonyl compounds

Syntheses of 5-halogeno-2,4-dienals 1a-c are described starting either from the glutaconaldehyde potassium salt or from furan. The 5-bromopenta-2,4-dienal 1b can be transformed efficiently into homologous ω-bromo polyenals 2-4, precursors of ω-bromo polye