293732-19-1

Basic information

• Product Name: Benzene, 1-(bromomethyl)-2-iodo-4,5-dimethoxy-
• CAS NO: 293732-19-1
• Molecular Formula: C9H10BrIO2
• Molecular Weight: 356.986
• Mol File: 293732-19-1.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzene, 1-(bromomethyl)-2-iodo-4,5-dimethoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(bromomethyl)-2-iodo-4,5-dimethoxy-(293732-19-1)
• EPA Substance Registry System: Benzene, 1-(bromomethyl)-2-iodo-4,5-dimethoxy-(293732-19-1)

Safety Data

• Hazardous Substances Data: 293732-19-1(Hazardous Substances Data)

Upstream product

• 110451-87-1 2-bromomethyl-1-iodo-4,5-dimethoxybenzene 
• 93-03-8 (3,4-dimethoxyphenyl)methanol 
• 58432-83-0 (4,5-dimethoxy-2-iodophenyl)methyl chloride 

Downstream Products

• 293732-31-7 1-(2-iodo-4,5-dimethoxybenzyl)pyrrole-2-carboxylic acid diethyl amide 
• 299215-79-5 (E)-1-(2-bromophenyl)-N,N-dimethyl-2-(4,5-dimethoxy-2-iodophenyl)ethenylamine 
• 299215-77-3 (E)-N,N-dimethyl-2-(4,5-dimethoxy-2-iodophenyl)-1-(2-iodophenyl)ethenylamine 
• 299215-71-7 (E)-1,2-bis(4,5-dimethoxy-2-iodophenyl)-N,N-dimethylethenylamine 
• 445006-98-4 3-(2-iodo-4,5-dimethoxyphenyl)-2,2-dimethylpropanenitrile 
• 495414-19-2 3-(2-iodo-4,5-dimethoxyphenyl)-2,2-diphenylpropanenitrile 
• 524024-83-7 1-(2-iodo-4,5-dimethoxybenzyl)pyrrole-2-carboxylic acid methoxy methyl amide 
• 851384-83-3 [1-(2-iodo-4,5-dimethoxy-benzyl)-1H-pyrrol-2-yl]-morpholin-4-yl-methanone 
• 58432-84-1 2-(2-iodo-4,5-dimethoxyphenyl)acetonitrile 
• 916977-11-2 1-iodo-2-iodomethyl-4,5-dimethoxybenzene 
• 916977-18-9 methyl 7-(2-iodo-4,5-dimethoxybenzyl)-1-trimethylsiloxybicyclo[4.1.0]heptane-7-carboxylate 
• 916977-23-6 methyl 7-(4,5-dimethoxy-2-vinylbenzyl)-1-trimethylsiloxybicyclo[4.1.0]heptane-7-carboxylate 

Relevant articles and documents

Enantioselective Palladium-Catalyzed Heck-Heck Cascade Reactions: Ready Access to the Tetracyclic Core of Lycorane Alkaloids

A rapid and efficient access to a wide variety of enantiomerically enriched C-11b substituted lycorane analogues can be achieved via a catalytic asymmetric Heck-Heck 6-exo/6-endo cascade reaction in the presence of (R)-BINAP.

An efficient entry to pyrrolo[1,2-b]isoquinolines and related systems through Parham cyclisation

Aryllithiums generated by lithium-iodine exchange undergo intramolecular cyclisation to give pyrrolo[1,2-b]isoquinolines, in high yields. The best results were obtained when Weinreb or morpholine amides were used as internal electrophiles. The procedure h

Parham-type cycliacylation with Weinreb amides. Application to the synthesis of fused indolizinone systems

(Matrix presented) Weinreb amides behave as efficient internal electrophiles in Parham-type cycliacylation reactions. Thus, aryl- and heteroaryllithiums generated by lithium-halogen exchange undergo intramolecular cyclization to give fused indolizinone systems as pyrrolo[1,2-b]isoquinolines, thieno[2,3-f]indolizinones, and pyrrolo[1,2-b]acridinones in high yields.