148808-17-7

Basic information

• Product Name: 1,3-dimethoxy-5-<10-(2-tetrahydropyranyloxy)decanyl>benzene
• Synonyms: 1,3-dimethoxy-5-<10-(2-tetrahydropyranyloxy)decanyl>benzene
• CAS NO: 148808-17-7
• Molecular Weight: 378.552
• Mol File: 148808-17-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,3-dimethoxy-5-<10-(2-tetrahydropyranyloxy)decanyl>benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-dimethoxy-5-<10-(2-tetrahydropyranyloxy)decanyl>benzene(148808-17-7)
• EPA Substance Registry System: 1,3-dimethoxy-5-<10-(2-tetrahydropyranyloxy)decanyl>benzene(148808-17-7)

Safety Data

• Hazardous Substances Data: 148808-17-7(Hazardous Substances Data)

Upstream product

• 13019-22-2 9-Decen-1-ol 
• 70863-80-8 9-((tetrahydro-2H-pyran-2-yl)oxy)nonan-1-al 
• 67136-13-4 1-(tetrahydro-2-pyranyloxy)-9-decene 
• 110-87-2 3,4-dihydro-2H-pyran 
• 148808-16-6 1,3-dimethoxy-5-<10-(2-tetrahydropyranyloxy)-1-decenyl>benzene 

Downstream Products

• 148808-20-2 2-bromo-5-methoxy-3-<(Z)-10'-pentadecenyl>-1,4-benzoquinone 
• 148808-21-3 1,4-dihydroxy-2-methoxy-6-<(Z)-10'-pentadecenyl>benzene 
• 97987-89-8 belamcandaquinone 
• 148808-18-8 2-Bromo-5-methoxy-3-((Z)-pentadec-10-enyl)-phenol 
• 137786-93-7 belamcandaphenol 
• 137786-94-8 belamcandol B 
• 137786-97-1 10-(3,5-dimethoxyphenyl)decanal 
• 87746-51-8 dimethoxymaesanin 
• 82380-21-0 maesanin 
• 34809-61-5 1,3-dimethoxy-5-<(Z)-10'-pentadecenyl>benzene 
• 152430-95-0 10-(3,5-Dimethoxy-phenyl)-decan-1-ol 

Relevant articles and documents

Naturally occurring 5-lipoxygenase inhibitor. II. Structures and syntheses of ardisianones A and B, and maesanin, alkenyl-1,4-benzoquinones from the rhizome of Ardisia japonica

New alkenyl-1,4-benzoquinones, ardisianones A (1) and B (2), and the known maesanin (3) as 5-lipoxygenase inhibitors have been isolated from the rhizome of Ardisia japonica. Their structures have been elucidated as 2-methoxy-6-[(Z)-10'-pentadecenyl]-1,4-benzoquinone and 5-hydroxy-2-methoxy-6-[(Z)-8'-tridecenyl]-1,4-benzoquinone, respectively, on the basis of spectroscopic data and chemical degradation. Ardisianone A (1), maesanin (3) and belamcandol A (7) have been synthesized starting from belamcandol B (6), readily prepared by Wittig reaction between 9-(2-tetrahydropyranyloxy)nonanal and 3,5-dimethoxybenzyltriphenylphosphonium bromide followed by selective demethylation with sodium thioethoxide.