88865-35-4

Upstream product

• 88865-34-3 (E)-4-(4-methoxyphenoxy)-2-methyl-2-buten-1-ol 
• 55514-49-3 ethyl (E)-γ-bromo-α-methylbut-2-enoate 
• 88865-33-2 ethyl (E)-4-(4-methoxyphenoxy)-2-methyl-2-butenoate 
• 150-76-5 4-methoxy-phenol 

Downstream Products

• 78957-33-2 (E)-2,6-dimethyl-8-(4-methoxyphenoxy)-6-octen-3-yne-2,5-diol 
• 88865-39-8 2,2-dimethyl-5-<(E)-3-(4-methoxyphenoxy)-1-methyl-1-propenyl>-3(2H)-furanone 
• 78957-40-1 3-acetoxy-2,2-dimethyl-5-<(E)-3-(4-methoxyphenoxy)-1-methyl-1-propenyl>-2,5-dihydrofuran 
• 88865-36-5 (E)-5-acetoxy-2,6-dimethyl-8-(4-methoxyphenoxy)-6-octen-3-yn-2-ol 

Relevant academic research and scientific papers

Regiocontrolled Formation of 4,5-Dihydro-3(2H)-furanones from 2-Butyne-1,4-diol Derivatives. Synthesis of Bullatenone and Geiparvarin

Two new methods for selective hydration of 1,1,4-trisubstituted 2-butyne-1,4-diols (1) to give 4,5-dihydro-3(2H)-furanone derivatives are reported.The first involves selective monoacetylation of the less hindered hydroxyl group of 1 followed by Ag(I)-cata

4-Phenoxy-2-butene derivatives as plant growth regulators

4-Phenoxy-2-butene derivatives are disclosed as inhibitors of cytokinin plant growth regulatory activity and as possessing seed germination regulatory properties and senescence delaying activity when applied to plants. 4-Phenoxy-2-butene derivatives can also be useful as plant dwarfing agents, agents to retard seedling development or as herbicides.