34132-25-7

Basic information

• Product Name: Benzene, 2-bromo-1-(bromomethyl)-3,5-dimethoxy-
• CAS NO: 34132-25-7
• Molecular Formula: C9H10Br2O2
• Molecular Weight: 309.985
• Mol File: 34132-25-7.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzene, 2-bromo-1-(bromomethyl)-3,5-dimethoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 2-bromo-1-(bromomethyl)-3,5-dimethoxy-(34132-25-7)
• EPA Substance Registry System: Benzene, 2-bromo-1-(bromomethyl)-3,5-dimethoxy-(34132-25-7)

Safety Data

• Hazardous Substances Data: 34132-25-7(Hazardous Substances Data)

Upstream product

• 74726-76-4 2-bromo-3,5-dimethoxybenzyl alcohol 
• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 705-76-0 3,5-dimethoxybenzyl alcohol 
• 877-88-3 3,5-dimethoxybenzyl bromide 

Downstream Products

• 959618-99-6 C₂₅H₃₀BrN₃O₆ 
• 676596-82-0 (E)-2-bromo-1,5-dimethoxy-3-(4-methoxystyryl)benzene 
• 1400655-49-3 (3,5-dimethoxyphenyl)(3,5,7-trimethoxyphenanthren-9-yl)methanone 
• 1400655-53-9 1-(3,5-dimethoxyphenyl)-2-(4-methoxyphenyl)-1-(3,5,7-trimethoxyphenanthren-9-yl)ethanol 
• 1400655-48-2 (E)-10-(1-(3,5-dimethoxyphenyl)-2-(4-methoxyphenyl)vinyl)-2,4,6-trimethoxyphenanthrene 
• 1400655-58-4 (Z)-10-(1-(3,5-dimethoxyphenyl)-2-(4-methoxyphenyl)vinyl)-2,4,6-trimethoxyphenanthrene 
• 1400655-54-0 5-(3,5-dimethoxyphenyl)-1,3,9-trimethoxy-4-(4-methoxyphenyl)acephenanthrylene 
• 1400655-57-3 3,5,7,11,13-pentamethoxy-9-(4-methoxybenzyl)-9H-indeno-[2,1-l]phenanthrene 
• 921930-95-2 2-(2-bromo-3,5-dimethoxyphenyl)acetonitrile 
• 959619-01-3 C₃₀H₄₀BrN₃O₆ 
• 959619-00-2 C₂₇H₃₄BrN₃O₆ 
• 1449388-22-0 N-(2-bromo-3,5-dimethoxybenzyl)-N-methylnaphthalen-1-amine 
• 1449388-35-5 N-(2-bromo-3,5-dimethoxybenzyl)-N-(naphthalen-1-yl)benzamide 
• 268550-11-4 diethyl 2-bromo-3,5-dimethoxybenzyl phosphonate 

Relevant articles and documents

Total synthesis of laetevirenol A

The first complete synthesis of laetevirenol A was performed in nine steps via intramolecular Friedel-Crafts alkylation in a trans-selective manner. The key phenanthrene intermediate was synthesized by a one-pot Suzuki-Miyaura coupling and an aldol condensation cascade reaction.

SYNTHESIS OF RESVERATROL-BASED NATURAL PRODUCTS

Processes for synthesizing reveratrol-based oligomers are provided. In addition, reservatrol-based oligomer compounds free of plant extract are provided.

IMIDAZOAZEPHINONE COMPOUNDS

The invention relates to compounds of formula (I): along with pharmaceutical compositions containing the same and methods of use thereof.