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Usage

Uses

Used in Perfumery Industry:
2,4,6-Heptatrienal, 7-(4-methoxyphenyl)-, (E,E,E)is used as a fragrance ingredient for its strong floral, rose-like scent, enhancing the olfactory profiles of various perfumes and colognes.
Used in Food Industry:
In the food industry, 2,4,6-Heptatrienal, 7-(4-methoxyphenyl)-, (E,E,E)serves as a flavoring agent, imparting a unique and pleasant taste to different food products, thereby enhancing their overall sensory appeal.
Used in Personal Care and Cosmetic Products:
2,4,6-Heptatrienal, 7-(4-methoxyphenyl)-, (E,E,E)is used as an ingredient in personal care and cosmetic products due to its potential antioxidant properties, which can help protect the skin from oxidative stress and contribute to anti-aging effects.
Used in Antimicrobial Applications:
2,4,6-Heptatrienal, 7-(4-methoxyphenyl)-, (E,E,E)-'s antimicrobial properties make it a candidate for use in formulations designed to combat microbial growth, thus preserving the shelf life and safety of various products.
Used in Pesticide and Insect Repellent Formulations:
2,4,6-Heptatrienal, 7-(4-methoxyphenyl)-, (E,E,E)is studied for its potential use in natural pesticide and insect repellent formulations, offering an alternative to synthetic chemicals for pest control in agriculture and other settings.

Upstream product

• 24680-50-0 4-methoxy-trans-cinnamaldehyde 
• 129144-62-3 C₈H₁₁LiO 
• 123-11-5 4-methoxy-benzaldehyde 
• 129144-61-2 C₁₀H₁₇LiO₂ 
• 19493-09-5 Methylenetriphenylphosphorane 
• 82724-69-4 1-Methoxy-4-((1E,5E)-3,7,7-triethoxy-hepta-1,5-dienyl)-benzene 
• 82724-70-7 1,1,3,7-Tetraethoxy-7-(4-methoxyphenyl)-4-heptene 
• 49678-07-1 (2E,4E)-5-(4-methoxyphenyl)penta-2,4-dienal 
• 72233-10-4 3,3-Diethoxy-1-(4-methoxyphenyl)-(E)-1-propen 
• 82724-67-2 1,1,5-Triethoxy-5-(4-methoxyphenyl)-2-pentene 
• 53484-50-7 (E)-p-methoxy-cinnamyl alcohol 
• 3901-07-3 3-(4-methoxy-phenyl)acrylic acid methyl ester 
• 129144-74-7 6-bromo-1,1-diethoxyhexa-3E,5Z-diene 
• 154141-24-9 6-bromo-1-ethoxyhexa-1Z,3E,5Z-triene 

Downstream Products

• 111325-85-0 (+/-)-1ξ-methoxy-11t-(4-methoxy-phenyl)-undeca-1,6t,8t,10-tetraen-3-yn-5-ol 
• 79512-93-9 ethyl 9-(4-methoxyphenyl)-2,4,6,8-nonatetraenoate 
• 136795-73-8 1-p-Methoxyphenyl-8-p-nitrophenyl-1,3,5,7-octatetraen 
• 79512-87-1 11t-(4-methoxy-phenyl)-undeca-2t,4t,6t,8t,10-pentaenal 

Relevant academic research and scientific papers

Donor Rhodium Carbenes by Retro-Buchner Reaction

Rhodium carbenes are key intermediates in a range of cycloadditions and insertion reactions. Herein, we report the first generation of donor RhII carbenes by decarbenation of 7-substituted 1,3,5-cycloheptatrienes. This discovery unlocks an improved retro-Buchner-cyclopropanation sequence, a Si?H insertion reaction for a broad-scope synthesis of allylsilanes, and a new method for the vinylogation of aldehydes. The last strategy led to the development of an iterative synthesis of E-polyenes, and to the total synthesis of navenones B and C.

Facile One Pot Thermal Dehydration and Dethioacetalization of β-Hydroxydithioacetals with Dimethyl sulphoxide: Synthesis of α,β-Unsaturated Aldehydes

The acyclic and cyclic β-hydroxydithioacetals 3a-m and 4a-b obtained by sodium borohydride reduction (or Grignard addition) of the corresponding β-oxodithioacetals 2a-m are shown to undergo facile one pot thermal dehydration and dethioacetalization in the presence of dimethyl sulphoxide to afford the corresponding ene- and polyene aldehydes 5a-m and 6a-b in good yields.The probable mechanism of dethioacetalization with dimethyl sulphoxide has also been discussed.

Reactivity of polyvinylogation: Easy and rapid access to different polyenals

This work describes the synthesis and the reactivity of three reagents of polyvinylogation 1-3. By condensation with several aldehydes and ketones, these reagents allow the introduction of three or four doubles bonds, leading to polyenals 5-6 in one or tw

CHEMISTRY OF ENOL ETHERS. LVI. CONDENSATION OF THE ACETALS OF AROMATIC ALDEHYDES WITH 1-ETHOXY-1,3-BUTADIENE. SYNTHESIS OF ARYLPOLYENE ALDEHYDES

The condensation of a series of acetals of aromatic aldehydes (benzaldehyde, 4-methoxy and 3,4-dimethoxybenzaldehyde) with 1-ethoxy-1,3-butadiene was investigated.Successful realization of the reaction requires the presence of electron-donating goups in t