1006268-64-9 Usage
Description
(2E)-1-(4-aminophenyl)-3-(4-hydroxy-2-methoxyphenyl)prop-2-en-1-one is a complex organic compound that features a prop-2-en-1-one backbone with a 4-aminophenyl and a 4-hydroxy-2-methoxyphenyl group attached to it. Classified as a ketone, this molecule is notable for its electron-donating capability as a nucleophile. Its unique structural features suggest potential biological and pharmacological relevance, possibly allowing interactions with specific biological targets and exhibiting drug-like properties. Further exploration and analysis are required to uncover the full spectrum of its applications and effects.
Uses
Used in Pharmaceutical Development:
(2E)-1-(4-aminophenyl)-3-(4-hydroxy-2-methoxyphenyl)prop-2-en-1-one is utilized as a key intermediate in the synthesis of pharmaceuticals, particularly for drugs targeting various diseases. Its structural attributes, including the presence of an electron-donating ketone group and the potential for hydrogen bonding, make it a promising candidate for the development of new therapeutic agents.
Used in Chemical Research:
In the field of chemical research, (2E)-1-(4-aminophenyl)-3-(4-hydroxy-2-methoxyphenyl)prop-2-en-1-one serves as a subject of study for understanding the reactivity and properties of complex organic molecules. Its unique structure allows researchers to investigate its potential as a nucleophile and its interactions with other molecules, which can contribute to the advancement of organic chemistry.
Used in Material Science:
(2E)-1-(4-aminophenyl)-3-(4-hydroxy-2-methoxyphenyl)prop-2-en-1-one may also find applications in material science, where its structural features could be leveraged to develop new materials with specific properties. For instance, its ability to donate electrons might be harnessed in the creation of conductive polymers or other electronic materials.
Note: The specific applications listed above are speculative and based on the general properties of the compound as described. Actual uses would depend on further research and development in relevant fields.
Check Digit Verification of cas no
The CAS Registry Mumber 1006268-64-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,6,2,6 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1006268-64:
(9*1)+(8*0)+(7*0)+(6*6)+(5*2)+(4*6)+(3*8)+(2*6)+(1*4)=119
119 % 10 = 9
So 1006268-64-9 is a valid CAS Registry Number.
1006268-64-9Relevant articles and documents
Chalcones, inhibitors for topoisomerase i and cathepsin B and L, as potential anti-cancer agents
Kim, Seok-Ho,Lee, Eunyoung,Baek, Kyung Hye,Kwon, Han Byeol,Woo, Hyunjung,Lee, Eung-Seok,Kwon, Youngjoo,Na, Younghwa
, p. 3320 - 3324 (2013/06/27)
In order to diversify the pharmacological activity of chalcones and extend the scaffold of topoisomerase and cathepsins B and L inhibitors, we have designed and synthesized total 18 chalcone compounds and tested their biological activity. In the topoisome
