5273-91-6

Upstream product

• 5273-79-0 2,4-dimethoxy-1-(prop-2-enyloxy)benzene 
• 74-88-4 methyl iodide 
• 100612-87-1 1-(2-allyl-3-hydroxy-4,6-dimethoxyphenyl)ethanone 
• 67-68-5 dimethyl sulfoxide 
• 121-33-5 vanillin 
• 20240-58-8 3-allyl-4-hydroxy-5-methoxybenzaldehyde 
• 22280-95-1 4-allyloxy-3-methoxybenzaldehyde 
• 77-78-1 dimethyl sulfate 
• 31788-39-3 2-methoxy-6-prop-2'-enylbenzene-1,4-diol 
• 13330-65-9 2,4-dimethoxyphenol 
• 106-95-6 allyl bromide 

Downstream Products

• 1312615-90-9 C₁₁H₁₅IO₃ 
• 1312615-89-6 C₁₁H₁₆O₄ 
• 1312615-88-5 C₁₁H₁₄O₄ 
• 1312615-93-2 C₁₈H₂₆O₄ 
• 1312615-91-0 C₁₇H₂₄O₄ 
• 5273-82-5 (E)-1,2,5-trimethoxy-3-(prop-1-en-1-yl)benzene 
• 5273-81-4 cis-2,3,5-Trimethoxy-1-propenyl-benzol 

Relevant academic research and scientific papers

Towards an asymmetric synthesis of the bacterial peptide deformylase (PDF) inhibitor fumimycin

Studies towards the synthesis of the bacterial peptide deformylase (PDF) inhibitor fumimycin are reported. The synthetic approach features an organocatalytic access to the α,α-disubstituted amino acid unit and results in the synthesis of an advanced inter

Synthesis and hypolipidemic and antiplatelet activities of α-asarone isomers in humans (in vitro), mice (in vivo), and rats (in vivo)

A series of α-asarone isomers was synthesized and investigated for their hypolipidemic and antiplatelet activity. Considering the hypolipidemic activity in rats at a dose of 80 mg/kg/day, some isomers were more potent than clofibrate at 150 mg/kg. Compoun

Feeding-deterrent activity of α-asarone isomers against some stored Coleoptera

All isomers of α-asarone [(E)-4-prop-1-enyl-1,2,5-trimethoxybenzene] were tested for their feeding deterrent activity against adults of Sitophilus granarius and Tribolium confusum and larvae of Trogoderma granarium and Tribolium confusum. (E)-2-prop-1-eny

Crystal structures of 1,2,5-trimethoxy-3-(1-propenyl)benzene and 1,3,5-trimethoxy-2-(1-propenyl)benzene

The crystal structures of 1,2,5-trimethoxy-3-(1-propenyl)benzene (D) and 1,3,5-trimethoxy-2-(1-propenyl)benzene (F) have been determined by X-ray diffraction methods. The compounds crystallize in the monoclinic system, space group P21/c for (D)

STRUCTURE-ACTIVITY RELATIONSHIPS OF PHENYLPROPANOIDS AS GROWTH INHIBITORS OF THE GREEN ALGA SELENASTRUM CAPRICORNUTUM

Twenty-seven commercial or synthetic phenylpropanoids have been tested in broth against the unicellular alga Selenastrum capricornutum.The antialgal activity seems to be linked to the number as well as to the position of the methoxyl group in the molecule.A slight effect of the side chain substitution was also observed. Key Word Index - Selenastrum capricornutum; allelochemicals; phenylpropanoids.