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3,7-bis-benzyloxy-2-(3,4-dimethoxy-phenyl)-5-methoxy-chromen-4-one is a complex organic compound characterized by its unique molecular structure. It features a chromen-4-one core, which is a type of chromone, a class of organic compounds that are derivatives of coumarin. The molecule is adorned with two benzyloxy groups at the 3 and 7 positions, which are benzyl ether functional groups that can protect hydroxyl groups during chemical reactions. Additionally, it has a 3,4-dimethoxy-phenyl group at the 2 position, contributing to its aromatic character and potentially influencing its physical and chemical properties. The 5-methoxy group further enhances the molecule's structure, adding to its complexity. 3,7-bis-benzyloxy-2-(3,4-dimethoxy-phenyl)-5-methoxy-chromen-4-one is likely to be used in the synthesis of pharmaceuticals or other organic compounds due to its intricate structure and the potential for further functionalization.

3306-18-1

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3306-18-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3306-18-1 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 3306-18:
(6*3)+(5*3)+(4*0)+(3*6)+(2*1)+(1*8)=61
61 % 10 = 1
So 3306-18-1 is a valid CAS Registry Number.

3306-18-1Relevant academic research and scientific papers

Quercetin derivative and its preparation method and application

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Paragraph 0074, (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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