39000-58-3

Upstream product

• 150-78-7 1,4-dimethoxybezene 
• 60-29-7 diethyl ether 
• 64-17-5 ethanol 
• 7664-41-7 ammonia 

Downstream Products

• 118658-77-8 2-<2-(2-naphtyl)ethyl>cyclohexane-1,4-dione 
• 86975-03-3 3-(2,5-Dimethoxy-phenyl)-4,7-dimethoxy-3H-isobenzofuran-1-one 
• 93832-29-2 methyl 2-formyl-3,6-dimethoxybenzoate diethyl acetal 
• 150-78-7 1,4-dimethoxybezene 
• 3840-27-5 2,5-dimethoxybenzyl chloride 
• 25224-72-0 1,4-dimethoxybenzene-2,6-dicarboxaldehyde 
• 172288-50-5 2-<2-(9-Phenanthryl)ethyl>cyclohexane-1,4-dione 
• 126838-56-0 methyl 3,6-dimethoxy-2-methylbenzoate 
• 12116-44-8 (η6-anisol)tricarbonyl chromium 
• 129248-54-0 2-[2-(5-Methoxy-1-naphtyl)ethyl]cyclohexan-1,4-dione 
• 216664-12-9 1,3-bis[2-(2,5-diketocyclohexyl)ethyl]benzene 
• 637-88-7 1,4-Cyclohexanedione 
• 931-57-7 1-methoxy-cyclohex-1-ene 
• 81722-06-7 ethyl 2,5-dimethoxy benzoate 

Relevant academic research and scientific papers

Enantioselective hydride abstraction in organic substrates: A novel use for chiral carbenium ions

(Matrix presented) It is surprising that chiral cations have not been used to distinguish between prochiral hydrides when converse notions, such as asymmetric addition of a hyride to a prochiral functional group or use of a chiral anion to distinguish bet

Ammonia-free Birch reductions with sodium stabilized in silica gel, Na-SG(I)

Ammonia-free Birch reduction conditions were developed based upon sodium stabilized in silica gel for a variety of substrates. In general, the yields were similar to those reported for lump sodium in liquid ammonia.