855839-06-4

Basic information

• Product Name: 1,1′-(2-hydroxy-4,6-dimethoxy-1,3-phenylene)bis(ethan-1-one)
• Synonyms: 1,1′-(2-hydroxy-4,6-dimethoxy-1,3-phenylene)bis(ethan-1-one)
• CAS NO: 855839-06-4
• Molecular Weight: 238.24
• Mol File: 855839-06-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1,1′-(2-hydroxy-4,6-dimethoxy-1,3-phenylene)bis(ethan-1-one)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1′-(2-hydroxy-4,6-dimethoxy-1,3-phenylene)bis(ethan-1-one)(855839-06-4)
• EPA Substance Registry System: 1,1′-(2-hydroxy-4,6-dimethoxy-1,3-phenylene)bis(ethan-1-one)(855839-06-4)

Safety Data

• Hazardous Substances Data: 855839-06-4(Hazardous Substances Data)

Upstream product

• 2161-86-6 2,4-diacetylphloroglucinol 
• 74-88-4 methyl iodide 
• 621-23-8 1,2,3-trimethoxybenzene 
• 75-36-5 acetyl chloride 
• 860688-04-6 2,4-diacetyl-1-benzyloxy-3,5-dimethoxy-benzene 
• 500-99-2 3,5-dimethoxyphenol 
• 7647-01-0 hydrogenchloride 
• 7446-70-0 aluminium trichloride 
• 90-24-4 2-hydroxy-4,6-dimethoxyacetophenone 
• 60-29-7 diethyl ether 
• 75-05-8 acetonitrile 
• 108-24-7 acetic anhydride 
• 72221-04-6 2,4-Diacetyl-3,5-dimethoxy-phenol 

Downstream Products

• 855462-43-0 [5-hydroxy-7-methoxy-2-(4-methoxy-phenyl)-4-oxo-4H-chromen-8-yl]-acetic acid 

Relevant articles and documents

Synthesis, biological evaluation and molecular docking studies of bis-chalcone derivatives as xanthine oxidase inhibitors and anticancer agents

In this study, a series of B-ring fluoro substituted bis-chalcone derivatives were synthesized by Claisen-Schmidt condensation reactions and evaluated for their ability to inhibit xanthine oxidase (XO) and growth inhibitory activity against MCF-7 and Caco

Multi-substituted aromatic diketone compound and its preparation method and application (by machine translation)

The invention of the formula (I) of the said multi-substituted aromatic diketone compound and its preparation and application. Formula (I) in R 1 formula (I-1), type (I-2) or a formula (I-3) substituent, R 2 to-H, -F, -Cl, -Br, -CH 3 or-OCH 3. When the R 1 formula (I-1) time, the method of the invention is to 2,4-di-hydroxy acetophenone as raw materials, and the bromine acetaldehyde compressed ethylene glycol reaction to obtain 1 - (4 - (2,2-methoxyethoxy) - 2-hydroxy-phenyl) ethanone, then the ring, and aryl acyl chloride reaction, the rearranged under alkaline conditions to obtain multi-substituted aromatic diketone compound. When the R 1 (I-2) for the time, the method of this invention and R 1 (I-1) is basically the same as the. When the R 1 formula (I-3) time, the method of the invention is to to phloroglucinol as raw materials, by methylation of 1, 3, 5-trimethoxy, by reaction with acetyl chloride 1,1 ˊ - (2-hydroxy -4,6-dimethoxy -1,3-phenylene) b ethanone, then the aryl acyl chloride reaction, the rearranged under alkaline conditions to obtain multi-substituted aromatic diketone compound. Compound of the present invention, to HIV-1 integrase inhibiting effect. (by machine translation)