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872595-57-8

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872595-57-8 Usage

Properties

1. Chemical Structure: Complex molecular structure consisting of a benzofuran derivative with a benzopyran ring.
2. Substituent: Contains a 4-methoxyphenylimino substituent.
3. Geometry: The imino group attached to the benzopyran ring is in the E configuration.
4. Functional Groups: Contains functional groups such as imino (-NH-) and methoxy (-OCH3).
5. Ring System: Comprised of a benzofuro and a benzopyran ring system.
6. Biological Activity: Potentially exhibits unique biological activities due to its structure.

Substituent Description

The substituent at the 4th position is an imino group derived from 4-methoxyphenyl.

Biological Impact

Suggests potential pharmacological and medicinal applications.

Therapeutic Potential

Could be explored for its effects on various biological processes.

Drug Development

May be of interest for further research in drug development.

This compound's intricate structure and potential biological activities make it a compelling subject for pharmaceutical and medicinal research, opening avenues for drug development and therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 872595-57-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,5,9 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 872595-57:
(8*8)+(7*7)+(6*2)+(5*5)+(4*9)+(3*5)+(2*5)+(1*7)=218
218 % 10 = 8
So 872595-57-8 is a valid CAS Registry Number.

872595-57-8Downstream Products

872595-57-8Relevant articles and documents

Synthesis and biological evaluation of functionalized coumarins as acetylcholinesterase inhibitors

Shen, Qiong,Peng, Quan,Shao, Jialiang,Liu, Xufeng,Huang, Zhishu,Pu, Xianzhang,Ma, Lin,Li, Yue-Ming,Chan, Albert S.C.,Gu, Lianquan

, p. 1307 - 1315 (2007/10/03)

Three series of functionalized coumarin compounds were designed and prepared as cholinesterase (AChE and BuChE) inhibitors. The biological profile against AChE and BuChE of the prepared compounds was determined. Compound 7b exhibited a mixed-type of AChE

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