89048-14-6

Basic information

• Product Name: Benzene, 1-(bromomethyl)-2,3,4,5-tetramethoxy-6-methyl-
• CAS NO: 89048-14-6
• Molecular Formula: C12H17BrO4
• Molecular Weight: 305.169
• Mol File: 89048-14-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzene, 1-(bromomethyl)-2,3,4,5-tetramethoxy-6-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(bromomethyl)-2,3,4,5-tetramethoxy-6-methyl-(89048-14-6)
• EPA Substance Registry System: Benzene, 1-(bromomethyl)-2,3,4,5-tetramethoxy-6-methyl-(89048-14-6)

Safety Data

• Hazardous Substances Data: 89048-14-6(Hazardous Substances Data)

Upstream product

• 89048-25-9 2,3,4,5-tetramethoxy-6-methyl benzaldehyde 
• 50-00-0 formaldehyd 
• 35896-58-3 2,3,4,5-tetramethoxytoluene 
• 72326-72-8 2-bromo-3,4,5-trimethoxy-1-methylbenzene 
• 6443-69-2 3,4,5-trimethoxytoluene 
• 86-81-7 3,4,5-trimethoxy-benzaldehyde 
• 123-63-7 paracetaldehyde 
• 3066-90-8 2,3-dimethoxy-5-methylbenzene-1,4-diol 
• 605-94-7 2,3-Dimethoxy-5-methyl-1,4-benzoquinone 
• 178262-70-9 2,3,4,5-tetramethoxy-6-methylphenylmethanol 

Downstream Products

• 129813-29-2 2,3-Dimethoxy-5-methyl-6-pyridin-3-ylmethyl-[1,4]benzoquinone 
• 1309779-61-0 bis-6-mercapmethyl bisubiquinone 
• 1319741-59-7 (6-thioacetylmethyl)ubiquinone 
• 1319741-60-0 4,5-dimethoxy-2-methy-3-thioacetylentyl-hydroquinone 
• 1319741-61-1 6-mercapmetyl hydroubiquinone 
• 1319741-58-6 2,3,4,5-tetramethoxy-6-(thioacetylmethyl)toluene 
• 89048-25-9 2,3,4,5-tetramethoxy-6-methyl benzaldehyde 
• 89048-58-8 2,3-dimethoxy-5-methyl-6-morpholinomethyl-1,4-benzoquinone 
• 129813-51-0 3-(2,3,4,5-Tetramethoxy-6-methyl-benzyl)-pyridine 

Relevant articles and documents

Practical synthesis of 2,3-dimethoxy-6-methyl-1,4-benzoquinone-5-carboxylic acid

2,3-Dimethoxy-6-methyl-1,4-benzoquinone-5-carboxylic acid was prepared in high yield by a reaction sequence starting from 2,3,4,5-tetramethoxytoluene (1) via a Blanc reaction, potassium dichromate oxidation, 30% H2O 2 oxidation and ceric ammonium nitrate oxidation.

Efficient synthesis of 2,3-dimethoxy-5-methyl-6-morpholinomethyl-1,4-benzoquinone hydrochloride

The title compound (5) was prepared by a reaction sequence starting from 2,3,4,5-tetramethoxytoluene (1) via the Blanc reaction, oxidation and alkylation. The described method provides a good yield of the C-6 heterocyclic-substituted benzoquinone derivati

Reversible redox of NADH and NAD+ at a hybrid lipid bilayer membrane using ubiquinone

Here, we report the reversible interconversion between NADH and NAD + at a low overpotential, which is in part mediated by ubiquinone embedded in a biomimetic membrane to mimic the initial stages of respiration. This system can be used as a platform to examine biologically relevant electroactive molecules embedded in a natural membrane environment and provide new insights into the mechanism of biological redox cycling.