82053-18-7

Basic information

• Product Name: Benzene, [(1E)-3-methoxy-1,5-hexadienyl]-
• CAS NO: 82053-18-7
• Molecular Formula: C13H16O
• Molecular Weight: 188.269
• Mol File: 82053-18-7.mol
• Article Data: 22

Chemical Properties

• CAS DataBase Reference: Benzene, [(1E)-3-methoxy-1,5-hexadienyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [(1E)-3-methoxy-1,5-hexadienyl]-(82053-18-7)
• EPA Substance Registry System: Benzene, [(1E)-3-methoxy-1,5-hexadienyl]-(82053-18-7)

Safety Data

• Hazardous Substances Data: 82053-18-7(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 103-26-4 Methyl cinnamate 
• 4407-36-7 (2E)-3-phenyl-2-propen-1-ol 
• 24808-73-9 (E)-(3-methoxyprop-1-en-1-yl)benzene 
• 762-72-1 allyl-trimethyl-silane 
• 24850-33-7 allyltributylstanane 
• 4364-06-1 cinnamaldehyde dimethylacetal 
• 72824-04-5 2-Allyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 14371-10-9 (E)-3-phenylpropenal 
• 4364-06-1 (E)-cinnamaldehyde dimethylacetal 
• 1825-61-2 Trimethylmethoxysilane 
• 149-73-5 trimethyl orthoformate 
• 79299-29-9 (E)-1-phenyl-1,5-hexadien-3-ol 
• 74-88-4 methyl iodide 

Downstream Products

• 106728-08-9 (E)-1,3-Diphenyl-octa-4,7-dien-1-one 
• 106728-07-8 1-Phenyl-3-((E)-styryl)-hex-5-en-1-one 
• 122800-50-4 Acetic acid (1R,4R)-3-benzyl-4-methoxy-cyclopent-2-enyl ester 
• 122800-48-0 acetic acid (2E,4E)-1-methyl-5-phenyl-penta-2,4-dienyl ester 
• 122800-49-1 Acetic acid (2E,4E)-1-acetoxymethyl-5-phenyl-penta-2,4-dienyl ester 
• 122800-42-4 (E)-1-((1-phenylhexa-1,5-dien-3-yloxy)methyl)benzene 
• 106728-05-6 2,2-Dimethyl-5-((E)-styryl)-oct-7-en-3-one 
• 106728-06-7 (E)-2,2-Dimethyl-5-phenyl-deca-6,9-dien-3-one 

Relevant articles and documents

Efficient Br?nsted acid catalyzed Hosomi-Sakurai reaction of acetals

Acetals react with allyltrimethylsilane in the presence of a catalytic amount of sulfonic acids to give the corresponding homoallylic ethers in high yields. The scope of the reaction is broad and both aromatic as well as aliphatic acetals can readily be u

Catalytic Use of Elemental Gallium for Carbon-Carbon Bond Formation

The first catalytic use of Ga(0) in organic synthesis has been developed by using a Ag(I) cocatalyst, crownether ligation, and ultrasonic activation. Ga(I)-catalyzed C-C bond formations between allyl or allenyl boronic esters and acetals, ketals, or aminals have proceeded in high yields with essentially complete regio- and chemoselectivity. NMR spectroscopic analyses have revealed novel transient Ga(I) catalytic species, formed in situ through partial oxidation of Ga(0) and B-Ga transmetalation, respectively. The possibility of asymmetric Ga(I) catalysis has been demonstrated.

Mesoporous aluminosilicate-catalyzed allylation of carbonyl compounds and acetals

A mesoporous aluminosilicate (Al-MCM-41) was found to be an effective heterogeneous catalyst for the reaction of both carbonyl compounds and acetals with allylsilanes to afford the corresponding homoallyl silyl ethers and homoallyl alkyl ethers, respectively. Both the mesoporous structure and the presence of aluminum moiety were indispensable for the high catalytic activity of Al-MCM-41. Moreover, Al-MCM-41 could catalyze the reaction of acetals chemoselectively in the presence of the corresponding carbonyl compounds. The solid acid catalyst Al-MCM-41 could be recovered easily by filtration and could be reused three times without a significant loss of catalytic activity.