1128-57-0

Basic information

• Product Name: Benzene, 1,2-dimethoxy-4,5-dimethyl-
• CAS NO: 1128-57-0
• Molecular Formula: C10H14O2
• Molecular Weight: 166.22
• Mol File: 1128-57-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzene, 1,2-dimethoxy-4,5-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,2-dimethoxy-4,5-dimethyl-(1128-57-0)
• EPA Substance Registry System: Benzene, 1,2-dimethoxy-4,5-dimethyl-(1128-57-0)

Safety Data

• Hazardous Substances Data: 1128-57-0(Hazardous Substances Data)

Upstream product

• 7721-62-2 4,5-dimethoxy-2-methylbenzaldehyde 
• 1134-52-7 1,2-Dimethoxy-4,5-bis(chloromethyl)benzene 
• 52806-46-9 1-bromo-4,5-dimethoxy-2-methylbenzene 
• 74-88-4 methyl iodide 
• 24932-48-7 1,2-dibromo-4,5-dimethylbenzene 
• 124-41-4 sodium methylate 
• 26726-81-8 1,2-bis(bromomethyl)-4,5-dimethoxybenzene 
• 91-16-7 1,2-dimethoxybenzene 
• 494-99-5 1,2-dimethoxy-4-methylbenzene 
• 67-56-1 methanol 
• 42117-30-6 2-methoxy-4,4-dimethylcyclohexa-2,5-dien-1-one 
• 2772-46-5 4,5-Dichlor-brenzcatechindimethylether 
• 917-54-4 methyllithium 
• 7537-05-5 1-(chloromethyl)-4,5-dimethoxy-2-methylbenzene 

Downstream Products

• 2785-74-2 4,5-dimethylbenzene-1,2-diol 
• 110274-91-4 3-bromo-1,2-dimethoxy-4,5-dimethyl-benzene 
• 117124-11-5 1,4-dibromo-2,3-dimethoxy-5,6-dimethyl-benzene 
• 26726-81-8 1,2-bis(bromomethyl)-4,5-dimethoxybenzene 
• 75833-54-4 3,6-dibromo-1,2-bisbromomethyl-4,5-dimethoxybenzene 
• 209911-11-5 1,4-Bis-chloromethyl-2,3-dimethoxy-5,6-dimethyl-benzene 
• 7771-25-7 2-methoxy-4,5-dimethylphenol 
• 100059-49-2 2,3-dimethoxy-5,6-dimethyl-benzoic acid 
• 209911-13-7 3,6-Bis-chloromethyl-4,5-dimethyl-benzene-1,2-diol 

Relevant articles and documents

Nucleophilic deoxyfluorination of catechols

Nucleophilic deoxyfluorinaiton of one of the two hydroxyl groups of catechols has been developed via the Umpolung concept. This method was successively applied to naturally occurring catechols, such as catechins and dopamine, to produce novel fluorinated

Highly substituted Schiff base macrocycles via hexasubstituted benzene: a convenient double Duff formylation of catechol derivatives

The synthesis of soluble, shape-persistent macrocycles is important for developing new materials. Double Duff formylation of 4,5-dialkylcatechol derivatives yields 3,6-diformyl-4,5-dialkylcatechols in moderate yields. These hexasubstituted aromatics are u

Chemistry of 2-Methoxy-2,5-cyclohexadienones. I. Photochemistry of 2-Methoxy-4,4-dimethyl-2,5-cyclohexadienone

The title compound, 2-methoxy-4,4-dimethyl-2,5-cyclohexadienone (V), was prepared from 2-methoxy-4,4-dimethyl-2-cyclohexenone (VIa).A methanolic solution of V was irradiated with a 200 W mercury lamp at -3 deg C to give 2,2-dimethoxy-6,6-dimethylbicyclo3