In 2002,Oliver, James E.; Doss, Robert P.; Marquez, Brian; DeVilbiss, E. David published 《Bruchins, plant mitogens from weevils: structural requirements for activity》.Journal of Chemical Ecology published the findings.Application In Synthesis of Methyl 3-hydroxypropanoate The information in the text is summarized as follows:
Bruchins are 3-hydroxypropanoate esters of long-chain α,ω-diols from pea weevils and cowpea weevils that have been shown to initiate callus formation on pea pods at extremely low application rates. Synthetic analogs have been prepared and examined to evaluate structural requirements for inducing this unusual neoplastic response. Chain length (optimum length C22-C24) is important, whereas unsaturation within the chain is relatively unimportant. Difunctionality is required for maximum activity, but the α,ω-diols themselves are inactive. Most critical is the ester portion(s) of the mols.; 3-hydroxypropanoate esters are far more active than any analogs examined In the part of experimental materials, we found many familiar compounds, such as Methyl 3-hydroxypropanoate(cas: 6149-41-3Application In Synthesis of Methyl 3-hydroxypropanoate)
Methyl 3-hydroxypropanoate(cas: 6149-41-3) belongs to esters with low molecular weight are commonly used as fragrances and found in essential oils and pheromones. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Application In Synthesis of Methyl 3-hydroxypropanoate
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics