105705-31-5

Basic information

• Product Name: Benzene, 2-bromo-1-(chloromethyl)-3,5-dimethoxy-
• CAS NO: 105705-31-5
• Molecular Formula: C9H10BrClO2
• Molecular Weight: 265.534
• Mol File: 105705-31-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, 2-bromo-1-(chloromethyl)-3,5-dimethoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 2-bromo-1-(chloromethyl)-3,5-dimethoxy-(105705-31-5)
• EPA Substance Registry System: Benzene, 2-bromo-1-(chloromethyl)-3,5-dimethoxy-(105705-31-5)

Safety Data

• Hazardous Substances Data: 105705-31-5(Hazardous Substances Data)

Upstream product

• 6652-32-0 3,5-dimethoxybenzylchloride 

Downstream Products

• 105705-18-8 benzyl miriquidate 
• 105705-35-9 2-(2-bromo-3,5-dimethoxybenzyl)propane-1,3-dioic acid 
• 105705-43-9 2,4-dimethoxy-66-(3-oxopentyl)benzoic acid 
• 105705-41-7 1-(2-bromo-3,5-dimethoxyphenyl)-3,3-diethoxypentane 
• 105705-39-3 1-(2-bromo-3,5-dimethoxyphenyl)pentan-3-one 
• 105705-37-1 3-(2-bromo-3,5-dimethoxyphenyl)propanoic acid 
• 105705-19-9 3-(2-Bromo-3,5-dimethoxy-phenyl)-propionyl chloride 
• 35578-70-2 miriquidic acid 
• 35583-00-7 2-hydroxy-4-methoxy-6-(3-oxopentyl)benzoic acid 
• 105705-33-7 diethyl 2-(2-bromo-3,5-dimethoxybenzyl)propane-1,3-dione 

Relevant articles and documents

NOVEL HETEROCYCLIC COMPOUNDS AS HSP90-INHIBITORS

Novel heterocyclic compounds are described and demonstrated to have utility as Heat Shock Protein 90 (HSP90) inhibiting agent. Method of synthesis and use of such compounds are also described.

Practical and regioselective brominations of aromatic compounds using tetrabutylammonium peroxydisulfate

Direct bromination of wide range of aromatic compounds substituted with electron donating groups such as methoxy, hydroxy, or amino groups have been achieved with high regioselectivity by the reaction with Br2 in the presence of tetrabutylammonium peroxydisulfate 1 under mild conditions in acetonitrile in excellent yields. The use of lithium bromide as a bromination reagent afforded high yields of monobromo compounds with complete regioselectivity under neutral and mild reaction conditions in acetonitrile.