72232-59-8

Basic information

• Product Name: 2,4,6-Heptatrienal, 7-(4-methoxyphenyl)-, (E,E,E)-
• CAS NO: 72232-59-8
• Molecular Formula: C14H14O2
• Molecular Weight: 214.264
• Mol File: 72232-59-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2,4,6-Heptatrienal, 7-(4-methoxyphenyl)-, (E,E,E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-Heptatrienal, 7-(4-methoxyphenyl)-, (E,E,E)-(72232-59-8)
• EPA Substance Registry System: 2,4,6-Heptatrienal, 7-(4-methoxyphenyl)-, (E,E,E)-(72232-59-8)

Safety Data

• Hazardous Substances Data: 72232-59-8(Hazardous Substances Data)

Usage

General Description

2,4,6-Heptatrienal, 7-(4-methoxyphenyl)-, (E,E,E)- is a chemical compound with the molecular formula C15H14O2. It is a yellowish liquid with a strong floral, rose-like odor. 2,4,6-Heptatrienal, 7-(4-methoxyphenyl)-, (E,E,E)- is often used in the production of perfumes and as a flavoring agent in the food industry. It is also known for its potential antioxidant and antimicrobial properties, making it a potentially useful ingredient in various personal care and cosmetic products. Additionally, this chemical has been studied for its potential applications in natural pesticide and insect repellent formulations.

Upstream product

• 3901-07-3 3-(4-methoxy-phenyl)acrylic acid methyl ester 
• 53484-50-7 (E)-p-methoxy-cinnamyl alcohol 
• 82670-30-2 E-5,5-diethoxy-2-pentenal 
• 146097-72-5 (4E,6E)-7-(4-Methoxy-phenyl)-1,1-bis-methylsulfanyl-hepta-4,6-dien-3-one 
• 82724-67-2 1,1,5-Triethoxy-5-(4-methoxyphenyl)-2-pentene 
• 72233-10-4 3,3-Diethoxy-1-(4-methoxyphenyl)-(E)-1-propen 
• 49678-07-1 (2E,4E)-5-(4-methoxyphenyl)penta-2,4-dienal 
• 82724-70-7 1,1,3,7-Tetraethoxy-7-(4-methoxyphenyl)-4-heptene 
• 82724-69-4 1-Methoxy-4-((1E,5E)-3,7,7-triethoxy-hepta-1,5-dienyl)-benzene 
• 123-11-5 4-methoxy-benzaldehyde 
• 19493-09-5 Methylenetriphenylphosphorane 
• 129144-61-2 C₁₀H₁₇LiO₂ 
• 129144-62-3 C₈H₁₁LiO 
• 24680-50-0 4-methoxy-trans-cinnamaldehyde 

Downstream Products

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

Relevant articles and documents

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.

A new route to trienals using 2-substituted 2H-pyran-based Wittig reagents

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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