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7-methoxy-3-(4-methoxyphenyl)-2H-chromene is a complex organic compound belonging to the class of flavones, characterized by a 2H-chromene core structure with a 7-methoxy group and a 4-methoxyphenyl substituent at the 3-position. This molecule is known for its potential biological activities, such as antioxidant and anti-inflammatory properties, which are attributed to its ability to modulate various cellular pathways. The presence of methoxy groups enhances its solubility and bioavailability, making it a subject of interest in pharmaceutical research for the development of new therapeutic agents.

4308-53-6

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4308-53-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4308-53-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,0 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4308-53:
(6*4)+(5*3)+(4*0)+(3*8)+(2*5)+(1*3)=76
76 % 10 = 6
So 4308-53-6 is a valid CAS Registry Number.

4308-53-6Relevant academic research and scientific papers

Iridium-Catalyzed Asymmetric Hydrogenation of 2H-Chromenes: A Highly Enantioselective Approach to Isoflavan Derivatives

Xia, Jingzhao,Nie, Yu,Yang, Guoqiang,Liu, Yangang,Zhang, Wanbin

supporting information, p. 4884 - 4887 (2017/09/23)

A highly efficient (aS)-Ir/In-BiphPHOX-catalyzed asymmetric hydrogenation of substituted 2H-chromenes and substituted benzo[e][1,2]oxathiine 2,2-dioxides is described. A series of 2H-chromenes and benzo[e][1,2]oxathiine 2,2-dioxides were hydrogenated to give the target products in high yields (92-99%) with excellent enantioselectivities (up to 99.7% ee) using our catalytic system. This reaction provides a direct and efficient method for the construction of chiral benzo six-membered oxygen-containing compounds.

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