114583-05-0

Basic information

• Product Name: 4-<14-(1',2'-dimethoxy-5'-tert-butylphenoxy)pentadecyl>veratrole
• CAS NO: 114583-05-0
• Molecular Weight: 540.827
• Mol File: 114583-05-0.mol

Chemical Properties

• CAS DataBase Reference: 4-<14-(1',2'-dimethoxy-5'-tert-butylphenoxy)pentadecyl>veratrole(CAS DataBase Reference)
• NIST Chemistry Reference: 4-<14-(1',2'-dimethoxy-5'-tert-butylphenoxy)pentadecyl>veratrole(114583-05-0)
• EPA Substance Registry System: 4-<14-(1',2'-dimethoxy-5'-tert-butylphenoxy)pentadecyl>veratrole(114583-05-0)

Safety Data

• Hazardous Substances Data: 114583-05-0(Hazardous Substances Data)

Upstream product

• 1129-21-1 4-t-butyl-1,2-benzoquinone 
• 77-78-1 dimethyl sulfate 
• 83532-40-5 3-<8'(Z),11'(E),13'(Z)-pentadecatrienyl>veratrole 

Relevant articles and documents

Coupling Reactions of 4-tert-Butyl-o-benzoquinone with Olefinic Compounds

Room-temperature bulk reactions of 4-tert-butyl-o-benzoquinone (5) and four alkenes, 1,4-pentadiene (6), methyl sorbate (7), methyl linoleate (8), and 3-veratrole (9) have been studied.Reactions with methylene-interrupted olefins 6, 8, and 9 afforded C-O and C-C linked 1:1 adducts through dehydrogenation paths, whereas the cycloaddition product 13 was exclusively produced by the reaction with 7.Comparing the product distribution of these reactions and the orientations predicted by the reactivities of possible reaction species, the hydride ion transfer mechanism has been inferred to dominate in the reaction of 5 and triene 9.On the other hand, the radical path involving the transfer of a hydrogen atom has been favored for reactions of 6 and 8.