223691-84-7

Basic information

• Product Name: 4-(4-methoxyphenyl)-4-methyl-hex-5-en-1-al
• Synonyms: 4-(4-methoxyphenyl)-4-methyl-hex-5-en-1-al
• CAS NO: 223691-84-7
• Molecular Weight: 218.296
• Mol File: 223691-84-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-(4-methoxyphenyl)-4-methyl-hex-5-en-1-al(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-methoxyphenyl)-4-methyl-hex-5-en-1-al(223691-84-7)
• EPA Substance Registry System: 4-(4-methoxyphenyl)-4-methyl-hex-5-en-1-al(223691-84-7)

Safety Data

• Hazardous Substances Data: 223691-84-7(Hazardous Substances Data)

Upstream product

• 401895-09-8 C₂₆H₃₂O₂ 
• 401895-11-2 C₁₉H₂₂N₂O₃S 
• 401895-13-4 toluene-4-sulfonic acid 3-(4-methoxy-phenyl)-3-methyl-cyclobutyl ester 
• 401895-07-6 1-methoxy-4-(3-methylhexa-1,5-dien-3-yl)benzene 
• 401895-12-3 3-(4-methoxy-phenyl)-3-methyl-cyclobutanol 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 75749-89-2 1-Methoxy-4-(1-methyl-cyclobut-2-enyl)-benzene 
• 1712-69-2 1-isopropenyl-4-methoxybenzene 
• 460323-49-3 2-(4-methoxy-phenyl)-2-methyl-5-methylene-cyclopentanol 
• 460323-47-1 1-(1,3-dimethyl-cyclopent-2-enyl)-4-methoxy-benzene 
• 460323-46-0 (E)-5-(4-Methoxy-phenyl)-hex-3-en-2-one 
• 50415-73-1 methyl 2-(4-methoxyphenyl)propionate 
• 23786-14-3 4-methoxy-phenyl acetic acid methyl ester 
• 252058-33-6 2-(4-methoxyphenyl)propanal 

Downstream Products

• 349473-22-9 4-(5,7-dimethylocta-1,6-dien-4-yl)phenol 
• 223691-88-1 1-(1,5-dimethyl-1-vinyl-hex-4-enyl)-4-methoxy-benzene 

Relevant articles and documents

Synthetic approaches to sporochnols A-C

Formal total synthesis of sporochnols A-C, hydroxyphenyl substituted monoterpenes isolated from the Caribbean brown alga Sporochnus bolleanus exhibiting feeding deterrent property toward herbivorous fish, is described. Copyright Taylor & Francis, Inc.

Total synthesis of sporochnols, fish deterrents from a marine alga

Sporochnols, fish deterrents from a marine alga, were synthesized, using intramolecular C-H insertion of alkylidenecarbene as a key step to construct the chiral quaternary center.