1100-15-8

Upstream product

• 39604-69-8 1-(2'-hydroxy-4',6'-dimethoxyphenyl)-2-(2,4-dimethoxyphenyl)ethanone 
• 109-94-4 formic acid ethyl ester 
• 149-73-5 trimethyl orthoformate 
• 36896-61-4 2,4-dimethoxyphenyllead triacetate 
• 110-91-8 morpholine 
• 4637-24-5 N,N-dimethyl-formamide dimethyl acetal 
• 153488-88-1 3-allyloxycarbonyl-5,7-dimethoxychroman-4-one 
• 54107-66-3 5,7-dimethoxy-4-chromanone 
• 521291-07-6 2,4,6,2',4'-pentamethoxy-deoxybenzoin 
• 139445-84-4 (2,4-dimethoxy-phenyl)-acetyl chloride 
• 6496-89-5 2,4-dimethoxyphenylacetic acid 
• 621-23-8 1,2,3-trimethoxybenzene 
• 153489-02-2 3-allyloxycarbonyl-5,7-dimethoxy-3-(2,4-dimethoxyphenyl)chroman-4-one 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 39604-69-8 1-(2'-hydroxy-4',6'-dimethoxyphenyl)-2-(2,4-dimethoxyphenyl)ethanone 
• 1156-78-1 2',4',5,7-tetrahydroxyisoflavone 
• 1100-14-7 3-(2,4-dimethoxy-phenyl)-5,7-dimethoxy-chroman-4-one 
• 98094-87-2 Lupinalbin A 
• 521291-07-6 2,4,6,2',4'-pentamethoxy-deoxybenzoin 
• 32884-36-9 5,2',4'-trihydroxy-7-methoxyisoflavone 

Relevant academic research and scientific papers

Total synthesis of apios isoflavones and investigation of their tyrosinase inhibitory activity

Apios isoflavone glucosides 1 and 2 were synthesized for the first time via Friedel–Crafts reaction, Bischler–Napieralski-type cyclization, and phase-transfer catalyzed glycosylation as the key steps. In addition, aglycones 4 and 5 and related natural iso

Constrained phytoestrogens and analogues as ERβ selective ligands

A new series of ERbeta (ERβ) selective ligands has been prepared. One of the compounds 6, structurally related to the phytoestrogen apigenin 4, displays a binding preference for ERβ over ERα of over 40-fold. In addition to its binding selectivity, 6 was a

Substituted 10,11-benzo[b]fluoren-10-ones as estrogenic agents

This invention provides estrogen receptor modulators of formula 1, having the structure wherein X, Y1, Y2, Y3, Y4, Z1, Z2, Z3, and Z4 are as defined in the specificati

Organolead-mediated Arylation of Allyl β-Ketoesters: A Selective Synthesis of Isoflavanones and Isoflavones

Arylation of A-ring substituted and unsabstituted 3-allyloxycarbonylchroman-4-ones with aryllead(IV) triacetates followed by selective catalytic deallyloxycarbonylation affords isoflavanones or isoflavones in high overall yields.The highest yield in the arylation step was observed in the reaction of 5,7-dimethoxychroman-4-one with the more hindered 2,4,6-trimethoxyphenyllead triacetate.

New 5-O-Methylisoflavones in the Roots of Yellow Lupin (Lupinus luteus L. cv. Barpine)

In addition to 5-O-methylgenistein (1), a further investigation of the isoflavonoid constituents in roots of the yellow lupin (Lupinus luteus L. cv.Barpine) has yielded five new 5-O-methylisoflavones named barpisoflavone A (2), 5-O-methyl-lupiwighteone (3