25315-69-9

Upstream product

• 87-13-8 diethyl 2-ethoxymethylenemalonate 
• 6921-34-2 benzylmagnesium chloride 
• 100-44-7 benzyl chloride 
• 100-39-0 benzyl bromide 

Downstream Products

• 1595262-47-7 C₁₉H₂₄O₂ 
• 1595262-56-8 C₃₁H₅₂O₂Si₂ 
• 1595262-53-5 C₃₁H₄₈O₂ 
• 859076-09-8 dibenzylmethylmalonic acid 
• 859202-24-7 amino-(1-benzyl-2-phenyl-ethyl)-malonic acid 
• 859076-69-0 (1-benzyl-2-phenyl-ethyl)-bromo-malonic acid 
• 858814-93-4 2-amino-3-benzyl-4-phenyl-butyric acid 
• 93651-70-8 3-benzyl-4-phenylbutanoic acid 

Relevant academic research and scientific papers

Design and synthesis of 2-(1,3-dialkoxy-2-methylpropan-2-yl)-1,3- diarylpropanes as tethering units for folded H-stacking polymers

1,3-Diarylpropenes 9 having a 1,3-dialkoxy-2-methylpropan-2-yl group were designed as tethering monomers for folded H-stacking polymers, and were readily synthesized from 2-ethoxymethylidene malonate in four- or five-steps, including a facile sequential a

Effect of deuterium on the kinetics of 1,5-hydrogen shifts: 5-Dideuteriomethylene-2,4,6,7,9-pentamethyl-11,11a-dihydro-12H-naphthacene

To obtain a more reliable temperature dependence of the kinetic deuterium isotope effect in a 1,5-hydrogen shift, the title compound has been designed to repress compromising side reactions, arguably arising from second-order ene-ene unions. The values of

A facile one-step synthesis of ethyl 2-(1,1-dialkyl and arylmethyl) malonates

Diethyl ethoxymethylenemalonate (EMME) is unexpectedly converted into diethyl 2-(1,1-dialkyl and diarylmethyl) malonate derivatives by a classical Grignard reaction. Addition of organocuprates to EMME gave diethyl 2-(1- ethoxyalkyl) malonate derivatives.