59056-76-7

Basic information

• Product Name: Benzene, 4-butyl-1,2-dimethoxy-
• Synonyms: 4-Butyl-1,2-dimethoxy-benzol;Benzene,4-butyl-1,2-dimethoxy;4-butyl-1,2-dimethoxy-benzene;4-Butyl-veratrol;4-n-butylveratrole
• CAS NO: 59056-76-7
• Molecular Formula: C12H18O2
• Molecular Weight: 194.274
• Mol File: 59056-76-7.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzene, 4-butyl-1,2-dimethoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 4-butyl-1,2-dimethoxy-(59056-76-7)
• EPA Substance Registry System: Benzene, 4-butyl-1,2-dimethoxy-(59056-76-7)

Safety Data

• Hazardous Substances Data: 59056-76-7(Hazardous Substances Data)

Upstream product

• 93-15-2 1,2-dimethoxy-4-(2-propenyl)benzene 
• 94-71-3 2-Ethoxyphenol 
• 64-17-5 ethanol 
• 120-80-9 benzene-1,2-diol 
• 90-05-1 2-methoxy-phenol 
• 91-16-7 1,2-dimethoxybenzene 
• 56880-86-5 4-(3,4-dimethoxyphenyl)butan-1-ol 
• 5906-99-0 2-nitrobenzenesulfonyl hydrazide 
• 2564-83-2 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical 
• 109-72-8 n-butyllithium 
• 65492-28-6 o-benzoquinone bis(dimethyl acetal) 
• 54419-21-5 1-(3,4-dimethoxyphenyl)butan-1-one 

Downstream Products

• 2525-05-5 1,2-dihydroxy-4-butylbenzene 
• 107275-71-8 2-butyl-4,5-dimethoxy-trans-cinnamic acid 
• 97742-35-3 5-oximino-1-n-butyl-3,4-dimethoxy-6,7,8,9-tetrahydro-5-H-benzocycloheptene 
• 76252-28-3 trans-4-(3′,4′-dimethoxyphenyl)but-3-ene 
• 97742-30-8 4-(2-n-butyl-4,5-dimethoxybenzoyl)-butyric acid 
• 100863-81-8 1-acetyl-2-butyl-4,5-dimethoxybenzene 
• 101589-34-8 2-butyl-4,5-dimethoxy-benzenesulfonic acid amide 
• 97758-99-1 4-(2-butyl-4,5-dimethoxy-phenyl)-4-oxo-butyric acid 

Relevant articles and documents

Site-Specific Alkene Hydromethylation via Protonolysis of Titanacyclobutanes

Methyl groups are ubiquitous in biologically active molecules. Thus, new tactics to introduce this alkyl fragment into polyfunctional structures are of significant interest. With this goal in mind, a direct method for the Markovnikov hydromethylation of alkenes is reported. This method exploits the degenerate metathesis reaction between the titanium methylidene unveiled from Cp2Ti(μ-Cl)(μ-CH2)AlMe2 (Tebbe's reagent) and unactivated alkenes. Protonolysis of the resulting titanacyclobutanes in situ effects hydromethylation in a chemo-, regio-, and site-selective manner. The broad utility of this method is demonstrated across a series of mono- and di-substituted alkenes containing pendant alcohols, ethers, amides, carbamates, and basic amines.

A template-free approach to nanotube-decorated polymer surfaces using 3,4-phenylenedioxythiophene (PhEDOT) monomers

In this work, novel 3,4-phenylenedioxythiophene (PhEDOT) monomers with alkyl, branched, and aromatic substituents were synthesized and tested for their efficacy at forming surfaces with unique wetting properties and surface morphology without the aid of surfactants. Monomers with a naphthalene substituent clearly showed the highest capacity to stabilize gas bubbles (O2 or H2) formed in solution during electrodeposition from trace water, resulting in the formation of nanotubes. Variation in the resulting density, diameter, and height of nanotubes was demonstrated by varying the electropolymerization protocol, conditions, or electrolyte used. The wetting induced by the nanotube formation results in the surfaces formed having both high contact angles with water (W) and strong adhesion, despite all polymers being intrinsically hydrophilic. This one-step and easily tunable approach to nanotube formation has potential to advance applications in membrane design, water transport and harvesting, as well as sensor design.

Single-step process for the reductive deoxygenation of unhindered alcohols

-