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3,7-bis-benzyloxy-2-(3,4-dimethoxy-phenyl)-5-hydroxy-chromen-4-one is a complex organic compound belonging to the class of flavonoids, specifically flavones. This molecule is characterized by a chromen-4-one core structure, which features a benzopyran ring system with a carbonyl group at the 4-position. The compound has two benzyloxy groups attached at the 3 and 7 positions, which are electron-donating groups that can influence the molecule's reactivity and solubility. Additionally, it contains a 3,4-dimethoxy-phenyl group at the 2-position, which introduces two methoxy groups that can further modulate the compound's properties. The 5-hydroxy group provides an additional site for potential interactions. 3,7-bis-benzyloxy-2-(3,4-dimethoxy-phenyl)-5-hydroxy-chromen-4-one is of interest in the field of organic chemistry and may have potential applications in pharmaceuticals or as a precursor in the synthesis of other complex molecules.

3306-17-0

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3306-17-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3306-17-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,0 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3306-17:
(6*3)+(5*3)+(4*0)+(3*6)+(2*1)+(1*7)=60
60 % 10 = 0
So 3306-17-0 is a valid CAS Registry Number.

3306-17-0Downstream Products

3306-17-0Relevant academic research and scientific papers

Quercetin derivative and its preparation method and application

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Paragraph 0080, (2018/01/19)

The invention discloses a quercetin derivative and a preparation method and application thereof. The preparation method comprises the following steps: firstly using dichlorodiphenylmethane to protect quercetin o-diphenol hydroxyl, combining a benzyl protection group to obtain the selectively protected quercetin derivative, and then independently reacting with dimethyl sulfate, diethyl sulfate, allyl bromide, paratoluensulfonyl chloride and acetic anhydride respectively to generate corresponding quercetin derivatives. All of the prepared derivative compounds have NRK-49F proliferation activity inhibition superior to that of quercetin. The quercetin derivatives 20a-1, 14a-1 and 23d-1 compositely replaced by methyl and p-tosyl have higher inhibition NRK-49F proliferation activity, and the inhibition ratio respectively reaches 86.33%, 78.04% and 75.91%. Thus, the currently obtained quercetin derivative compounds have obvious inhibition effect on kidney fibroblast NRK-49F proliferation.

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