102879-22-1

Upstream product

• 13321-73-8 2-bromo-1,5-dimethoxy-3-methylbenzene 
• 4179-19-5 1,3-dimethoxy-5-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 academic research and scientific papers

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.

First total synthesis of antrocamphin A and its analogs as anti-inflammatory and anti-platelet aggregation agents

Naturally occurring antrocamphin A (1) is a potent anti-inflammatory compound from the edible fungus Antrodia camphorata (Taiwanofungus camphoratus), whose wild fruiting body is used as a valuable folk medicine in Taiwan. This study is the first total syn

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.