89779-23-7 Usage
Uses
Used in Pharmaceutical Industry:
(4-amino-2-ethoxy-1,3-thiazol-5-yl)(3,4-dihydroxyphenyl)methanone is used as a pharmaceutical candidate for its potential antidiabetic and antioxidant activity. It is being studied for its ability to manage diabetes and combat oxidative stress, which are significant factors in various diseases.
Used in Neurodegenerative Disease Treatment:
In the field of neurology, (4-amino-2-ethoxy-1,3-thiazol-5-yl)(3,4-dihydroxyphenyl)methanone is used as a potential therapeutic agent for the treatment of neurodegenerative diseases. Its properties are being investigated for their capacity to protect neurons and slow down disease progression.
Used in Anti-inflammatory and Immunosuppressive Applications:
(4-amino-2-ethoxy-1,3-thiazol-5-yl)(3,4-dihydroxyphenyl)methanone is also used as an anti-inflammatory and immunosuppressive agent. Research is being conducted to understand its effects on reducing inflammation and modulating the immune system, which could be beneficial in treating autoimmune diseases and conditions involving excessive inflammation.
Overall, (4-amino-2-ethoxy-1,3-thiazol-5-yl)(3,4-dihydroxyphenyl)methanone, with its promising properties, is a candidate for further research and development in medicinal chemistry, with potential applications spanning across various therapeutic areas.
Check Digit Verification of cas no
The CAS Registry Mumber 89779-23-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,7 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 89779-23:
(7*8)+(6*9)+(5*7)+(4*7)+(3*9)+(2*2)+(1*3)=207
207 % 10 = 7
So 89779-23-7 is a valid CAS Registry Number.
89779-23-7Relevant academic research and scientific papers
Fuchigami, Toshio,Yeh, Mou-Yung,Nonaka, Tsutomu,Tien, Hsien-Ju
, p. 3851 - 3852 (1983)
α-Halo derivatives of ketones, ester, and nitrile reacted readily with potassium ethoxythiocarbonylcyanamide to provide the corresponding 4-amino-2-ethoxythiazole compounds in good yields, while α-halo amide did not.In a similar manner, α,α'-dihalo ketone reacted with 2 equiv of alkoxythiocarbonylcyanamide and S-methyl N-cyanocarbamodithioate salts to give the corresponding bis(4-amino-5-thiazolyl) ketones.