129478-11-1

Basic information

• Product Name: 1-(3,5-dimethoxyphenyl)-1-heptanol
• Synonyms: 1-(3,5-dimethoxyphenyl)-1-heptanol
• CAS NO: 129478-11-1
• Molecular Weight: 252.354
• Mol File: 129478-11-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-(3,5-dimethoxyphenyl)-1-heptanol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3,5-dimethoxyphenyl)-1-heptanol(129478-11-1)
• EPA Substance Registry System: 1-(3,5-dimethoxyphenyl)-1-heptanol(129478-11-1)

Safety Data

• Hazardous Substances Data: 129478-11-1(Hazardous Substances Data)

Upstream product

• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 3761-92-0 n-hexylmagnesium bromide 
• 17213-57-9 3,5-dimethoxybenzoyl chloride 
• 111-25-1 1-bromo-hexane 

Downstream Products

• 171569-32-7 1,3-dimethoxy-5-(trans-1'-heptenyl)benzene 
• 205746-53-8 2-(3,5-dihydroxyphenyl)-2-hexyl-1,3-dithiolane 
• 205746-52-7 2-(3,5-dimethoxyphenyl)-2-hexyl-1,3-dithiolane 
• 205746-54-9 5-(2-Hexyl-[1,3]dithiolan-2-yl)-2-((1R,6R)-6-isopropenyl-3-methyl-cyclohex-2-enyl)-benzene-1,3-diol 
• 52483-31-5 1,3-dimethoxy-5-(7'-hydroxyheptyl)benzene 
• 500-67-4 spherophorol 
• 39192-51-3 1-(3,5-dimethoxyphenyl)heptan-1-one 
• 6121-64-8 5-n-heptyl resorcinol dimethyl ether 

Relevant articles and documents

Pharmacophoric requirements for cannabinoid side chains: Multiple bond and C1'-substituted Δ8-tetrahydrocannabinols

Accumulated evidence indicates that within the cannabinoid structure the aliphatic side chain plays a pivotal role in determining cannabimimetic activity. We describe the synthesis and affinities for the CB1 and CB2 receptors of a series of novel Δ8

5-Alkylresorcinols from Hakea trifurcata that cleave DNA

A dichloromethane extract of Hakea trifurcata that mediated relaxation of ?X174 replicative form DNA at micromolar concentrations in the presence of Cu2+ was resolved into six active components by bioassay-guided fractionation. Five of the acti