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The chemical compound "2H,6H-Benzo[1,2-b:5,4-b']dipyran-6-one,10-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)-methyl]-7,8-dihydro-5-hydroxy-2,2-dimethyl-8-phenyl-" is a complex organic molecule with a unique structure. It features a benzodipyran-6-one core, which is a type of chromone, a class of compounds known for their diverse biological activities. The molecule is characterized by a 7,8-dihydro-5-hydroxy-2,2-dimethyl-8-phenyl group, which adds to its complexity and potential pharmacological properties. The presence of a 3-acetyl-2,4,6-trihydroxy-5-methylphenyl group attached to the molecule through a methyl bridge suggests that it may have significant chemical reactivity and could be involved in various biochemical processes. 2H,6H-Benzo[1,2-b:5,4-b']dipyran-6-one,10- [(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)- methyl]-7,8-dihydro-5-hydroxy-2,2- dimethyl-8-phenyl- 's intricate structure and functional groups make it a subject of interest for researchers in the fields of organic chemistry and pharmacology, potentially offering insights into new drug development or chemical synthesis strategies.

521-91-5

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521-91-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 521-91-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 521-91:
(5*5)+(4*2)+(3*1)+(2*9)+(1*1)=55
55 % 10 = 5
So 521-91-5 is a valid CAS Registry Number.

521-91-5Relevant academic research and scientific papers

The Mosaic of Rottlerin: The Sequel

Hong, Kenneth K. C.,Ho, Kitty K. K.,Bhadbhade, Mohan,Ball, Graham E.,Black, David Stc.,Kumar, Naresh

, p. 1190 - 1199 (2019/05/17)

Rottlerin (1) is a potent protein kinase C δinhibitor that possesses a wide range of biological activities. However, the potential of this molecule to be developed as a drug has been restricted by its limited availability. We report herein a gram scale quantity synthesis of rottlerin in a five-step synthetic route that can be completed within 2 days. The methodology was extended by the reaction of the key aminochromene intermediate (15) with various electron-rich arenes, forming novel unsymmetrical methylene-bridged compounds. The X-ray crystal structure revealed the boomerang shape of this kind of molecule for the first time. The direct transformation of rottlerin (1) into the natural product, isorottlerin (35), was observed for the first time, and we named this transformation the "isorottlerin change". In addition, the antibacterial activities of rottlerin (1) and new rottlerin analogues 32-34 were examined against Staphylococcus aureus. The compounds showed MIC values as low as 2.0 μM, which were comparable to the clinically used antibiotic gentamicin.

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