40926-76-9

Upstream product

• 6331-61-9 2-methoxy-4-(2-propenyl)phenoxyacetic acid 
• 97-53-0 4-allylguaiacol 

Downstream Products

• 135508-98-4 (3S,4R)-3-(4-Allyl-2-methoxy-phenoxy)-4-benzo[1,3]dioxol-5-yl-1-phenyl-azetidin-2-one 
• 135509-04-5 (3R,4S)-3-(4-Allyl-2-methoxy-phenoxy)-1-benzo[1,3]dioxol-5-ylmethyl-4-phenyl-azetidin-2-one 
• 100289-59-6 (3S,4R)-3-(4-Allyl-2-methoxy-phenoxy)-1,4-diphenyl-azetidin-2-one 
• 100289-62-1 (3S,4R)-3-(4-Allyl-2-methoxy-phenoxy)-1-(4-methoxy-phenyl)-4-phenyl-azetidin-2-one 
• 135509-01-2 (3R,4S)-3-(4-Allyl-2-methoxy-phenoxy)-4-benzo[1,3]dioxol-5-yl-1-(3,4-dimethoxy-benzyl)-azetidin-2-one 
• 135509-08-9 (3R,4S)-3-(4-Allyl-2-methoxy-phenoxy)-4-benzo[1,3]dioxol-5-yl-1-benzo[1,3]dioxol-5-ylmethyl-azetidin-2-one 
• 93149-03-2 (2-Methoxy-4-allyl-phenoxy)-essigsaeure-(N-ethoxy-N-ethyl-amid) 
• 92501-70-7 (2-Methoxy-4-allyl-phenoxy)-essigsaeure-(N-methoxy-N-methyl-amid) 

Relevant academic research and scientific papers

With herbicidal activity of 4 - benzoyl pyrazoles

The invention relates to a 4-benzoyl pyrazole compound with herbicidal activity. The structural formula of the 4-benzoyl pyrazole compound with the herbicidal activity is as shown in specifications, wherein R1 in the structural formula is selected from hy

Synthesis of Monocyclic β-Lactams with a Terpenoid Moiety

A series of new monocyclic β-lactams with a terpenoid moiety have been prepared by reaction of schiff bases with appropriate terpenyl acid chlorides in the presence of triethylamine.Their structural assignments are based on elemental analyses and spectral