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7-(benzyloxy)-2-(3,4-bis(benzyloxy)phenyl)-3-hydroxy-4H-chroMen-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

307521-01-3

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307521-01-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 307521-01-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,7,5,2 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 307521-01:
(8*3)+(7*0)+(6*7)+(5*5)+(4*2)+(3*1)+(2*0)+(1*1)=103
103 % 10 = 3
So 307521-01-3 is a valid CAS Registry Number.

307521-01-3Relevant academic research and scientific papers

BENZOPYRANONE DERIVATIVES AND THEIR USE AS ANTI-CORONAVIRAL AGENTS

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Page/Page column 34-35, (2008/06/13)

The invention relates to pharmaceutical compositions comprising benzopyranone derivatives for the treatment of Severe Acute Respiratory Syndrome (SARS).

Novel flavonoids

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, (2008/06/13)

Novel flavonoids of formula (I) 1where A and E form together a C—C or C=C bond; R1, R2, R3, and R4 are H, OH, O(CH2)n— aromatic group, n=0-8; O(CH2)n N(CH3)q with n=0-8, q=0-3; O(CH2)n OH with n=1-8; O(CH2)n-halide with n=1-8; O(CH2)n COOH with n=0-8; O(CH2)n COOR′ with n=0-8 and R′ is C1-C8 alkyl or an aromatic group; O(CH2)n CONH R″ with n=0-8 and R″ is C1-C8 alkyl or an aromatic group, and sugars in mono-, di- or trimeric form or analogues thereof, with the proviso that R1 is not H, at least two of R2, R3 and R4 are H, and at most one of R1, R2, R3 and R4 is OH, are useful for the treatment of drug-induced toxicity, doxorubicin-induced cardiotoxicity, free radical mediated diseases, lung diseases, cancer, diabetes mellitus, cardiovascular disease, or arteriosclerosis.

Synthesis of novel 3,7-substituted-2-(3',4'-dihydroxyphenyl)flavones with improved antioxidant activity

Van Acker,Hageman,Haenen,Van der Vijgh,Bast,Menge

, p. 3752 - 3760 (2007/10/03)

A series of 3,7-disubstituted-2-(3',4'-dihydroxyphenyl)flavones was synthesized as potential cardioprotective agents in doxorubicin antitumor therapy. The influence of substituents on the 3 and 7 positions of the flavone nucleus on radical scavenging and

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