88021-76-5 Usage
Uses
Used in Pharmaceutical Research and Development:
(E)-1-(2-hydroxyphenyl)-3-Morpholinoprop-2-en-1-one is used as a pharmaceutical candidate for its potential anti-cancer properties and enzyme inhibition capabilities. Its unique structure allows it to potentially interact with protein targets in the body, making it a valuable molecule for the development of new therapeutic agents.
Used in Organic Synthesis:
In the field of organic chemistry, (E)-1-(2-hydroxyphenyl)-3-Morpholinoprop-2-en-1-one is used as a key intermediate or building block for the synthesis of other organic compounds. Its distinctive structure and reactivity make it a versatile component in creating novel molecules with various applications.
Used in Cancer Treatment:
(E)-1-(2-hydroxyphenyl)-3-Morpholinoprop-2-en-1-one is used as an anti-cancer agent, targeting various types of cancer due to its potential to inhibit cancer cell growth and proliferation. Its effectiveness in this application is attributed to its ability to interact with and modulate specific biological targets within cancer cells.
Used in Enzyme Inhibition:
(E)-1-(2-hydroxyphenyl)-3-Morpholinoprop-2-en-1-one is utilized as an enzyme inhibitor, where it can potentially disrupt the activity of specific enzymes involved in various biological processes. This application is particularly relevant in the development of treatments for diseases where enzyme dysregulation plays a significant role.
Check Digit Verification of cas no
The CAS Registry Mumber 88021-76-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,2 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88021-76:
(7*8)+(6*8)+(5*0)+(4*2)+(3*1)+(2*7)+(1*6)=135
135 % 10 = 5
So 88021-76-5 is a valid CAS Registry Number.
88021-76-5Relevant academic research and scientific papers
Synthesis of 3,3-Dihalogenated 2-Aminochromanones via Tandem Dihalogenation and Cyclization of o-Hydroxyarylenaminones with NXS (X = Cl or Br)
Luo, Tian,Wu, Haozhi,Liao, Li-Hua,Wan, Jie-Ping,Liu, Yunyun
, p. 15785 - 15791 (2021/11/01)
An unprecedented method for the synthesis of dichlorinated and dibrominated 2-amino-substituted chromanones is developed by employing enaminones and NCS/NBS as starting materials under microwave irradiation. The reactions proceed quickly to deliver produc
Synthesis of polyfunctionalized benzophenones via the reaction of 3-formylchromones with tertiary push-pull enamines
Barkov, Alexey Yu.,Korotaev, Vladislav Yu.,Kutyashev, Igor B.,Sosnovskikh, Vyacheslav Ya.
, p. 2026 - 2033 (2016/04/05)
Uncatalyzed nucleophilic reaction of 3-formylchromones with tertiary push-pull enamines in refluxing acetonitrile gave polyfunctionalized benzophenone derivatives as a result of a [3+3] annulation in moderate to good yields.
Hetericyclic Systems. Part 14. Condensation Reactions of 2-(4-Oxo-4H-1-benzopyran-3-yl)-1,3-dioxolane
Ghosh, Chandra Kanta,Bandyopadhyay, Chandrakanta,Morin, Christophe
, p. 1989 - 1994 (2007/10/02)
Nitrogen nucleophiles under 1,4-addition with the title acetal (4; R=H, Me, and Cl) to give an intermediate that ultimately produces in most cases the same product as is obtained from the corresponding aldehyde (3) under similar conditions.Thus, compound
