35387-94-1

Basic information

• Product Name: Benzene, 2-iodo-1-methoxy-3-methyl-
• CAS NO: 35387-94-1
• Molecular Formula: C8H9IO
• Molecular Weight: 248.063
• Mol File: 35387-94-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzene, 2-iodo-1-methoxy-3-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 2-iodo-1-methoxy-3-methyl-(35387-94-1)
• EPA Substance Registry System: Benzene, 2-iodo-1-methoxy-3-methyl-(35387-94-1)

Safety Data

• Hazardous Substances Data: 35387-94-1(Hazardous Substances Data)

Upstream product

• 50868-73-0 2-methoxy-6-methylbenzeneamine 
• 100-84-5 1-methoxy-3-methyl-benzene 
• 5345-42-6 1-methoxy-3-methyl-2-nitro-benzene 

Downstream Products

• 1243471-41-1 2-iodo-3-methyl-phenol 
• 881846-30-6 1⁶,8⁶-dimethyl-1²,2²,3³,4²,5³,6²,7³,8²-octamethoxy-p-octiphenyl 
• 876384-12-2 (+/-)-5,6,7,8-tetrahydro-1-(2-methoxy-6-methylphenyl)-3-phenylisoquinoline-N-oxide 
• 876384-10-0 5,6,7,8-tetrahydro-1-(2-methoxy-6-methylphenyl)-3-phenylisoquinoline 
• 113137-97-6 4,4'''-dimethoxy-2,2'''-dimethyl-2',2'',4'',6'-tetranitro-m-quaterphenyl 
• 113138-07-1 (-)-3,7-di-isopropoxy-5-methoxy-4,6-bis(4-methoxy-2-methylphenyl)dibenzophosphole 5-oxide 
• 113138-07-1 (+)-3,7-di-isopropoxy-5-methoxy-4,6-bis(4-methoxy-2-methylphenyl)dibenzophosphole 5-oxide 
• 113138-07-1 (4R,5R,6S)-3,7-di-isopropoxy-5-methoxy-4,6-bis(4-methoxy-2-methylphenyl)dibenzophosphole 5-oxide 
• 113138-00-4 4'',6'-bis(diethylmethoxy)-4,4'''-dimethoxy-2,2'''-dimethyl-2',2''-dinitro-m-quaterphenyl 
• 113138-01-5 4'',6'-di-isopropoxy-4,4'''-dimethoxy-2,2'''-dimethyl-2',2''-dinitro-m-quaterphenyl 
• 113138-04-8 6'-isopropoxy-4,4'''-dimethoxy-2,2'''-dimethyl-2',2'',4''-trinitro-m-quaterphenyl 
• 113138-05-9 2'-isopropoxy-4,4'''-dimethoxy-2,2'''-dimethyl-2'',4'',6'-trinitro-m-quaterphenyl 
• 113138-03-7 4,4'''-Dimethoxy-2,2'''-dimethyl-4',2'',4''-trinitro-[1,3';1',1'';3'',1''']quaterphenyl-2'-ol 
• 113138-02-6 4,4'''-Dimethoxy-2,2'''-dimethyl-2',2'',4''-trinitro-[1,3';1',1'';3'',1''']quaterphenyl-4'-ol 

Relevant articles and documents

Expeditious synthesis of benzopyrans via lewis acid-catalyzed C-H functionalization: Remarkable enhancement of reactivity by an ortho substituent

An expeditious construction of a benzopyran skeleton via Lewis acid-catalyzed C-H functionalization was achieved. In this process, a [1,5] hydride shift and 6-endo cyclization successively occurred to give benzopyrans. The presence of substituents ortho to the alkoxy group significantly enhanced the reactivity, affording the desired compounds in excellent chemical yields with short reaction times.

Synthesis of the spirocyclic cyclohexadienone ring system of the schiarisanrins.

[structure: see text] Studies on the synthesis of the spirocyclic cyclohexadienone ring system 2 of the schiarisanrin family of natural products 1 are described and were based on the Lewis acid-promoted C-alkylation of the corresponding phenolic precursor.