102879-22-1

Basic information

• Product Name: Benzene, 2-iodo-1,5-dimethoxy-3-methyl-
• Synonyms: 2-iodo-3,5-dimethoxy-toluene;Benzene,2-iodo-1,5-dimethoxy-3-methyl;2-iodo-3,5-dimethyloxytoluene;2-Jod-3,5-dimethoxy-toluol
• CAS NO: 102879-22-1
• Molecular Formula: C9H11IO2
• Molecular Weight: 278.08700
• Mol File: 102879-22-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, 2-iodo-1,5-dimethoxy-3-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 2-iodo-1,5-dimethoxy-3-methyl-(102879-22-1)
• EPA Substance Registry System: Benzene, 2-iodo-1,5-dimethoxy-3-methyl-(102879-22-1)

Safety Data

• Hazardous Substances Data: 102879-22-1(Hazardous Substances Data)

Upstream product

• 4179-19-5 1,3-dimethoxy-5-methylbenzene 
• 13321-73-8 2-bromo-1,5-dimethoxy-3-methylbenzene 
• 72911-54-7 4-iodo-5-methyl-resorcinol 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 1262958-28-0 C₁₄H₁₆O₂ 
• 95868-15-8 10-acetyl-2-(2,4-dimethoxy-6-methyl-phenyl)-1,9-dimethyl-3-nitro-10H-phenoxazine 
• 94709-90-7 4-Amino-2.2'.4'-trimethoxy-5.6'-dimethyl-diphenylamin 
• 4946-96-7 2,2'-Dimethyl-4,4',6,6'-tetrahydroxy-biphenyl 
• 96808-59-2 N-(2-acetoxy-6-methyl-phenyl)-N-(2',4'-dimethoxy-2,6'-dimethyl-4,6-dinitro-biphenyl-3-yl)-acetamide 
• 96368-85-3 2-(2',4'-dimethoxy-2,6'-dimethyl-4,6-dinitro-biphenyl-3-ylamino)-3-methyl-phenol 

Relevant articles and documents

Studies of (Pd0-mediated) stille cross-coupling reactions of thiophenestannane with aryl halide derivatives

Stille (arylstannane) conditions used Pd0-mediated cross-coupling reactions for preparation of thiophene/aryl analogs. Different arylhalides were compared when coupled with heterometal (thiophenestannane) system. Comparable yields have now been obtained by Stille (arylstannane) couplings with different reactivity of arylhalides.

Halogenation of Phenols and Phenyl Ethers with Potassium Halides in the Presence of 18-Crown-6 on Oxidation with m-Chloroperbenzoic Acid

Several types of phenyl ethers have been monobrominated in the ring in good yields with potassium bromide in the presence of 18-crown-6 on oxidation with m-chloroperbenzoic acid.Monoiodination takes place with both phenyl ethers and free phenols when potassium iodide is employed.