52508-88-0 Usage
Uses
Used in Organic Chemical Synthesis:
5-Methoxy-2-oxoindoline-3-carbaldehyde is used as an intermediate in the production of various organic compounds, contributing to the synthesis of a wide range of chemical products.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 5-Methoxy-2-oxoindoline-3-carbaldehyde is utilized as an intermediate for the development of new drugs, thanks to its structural and functional properties that facilitate the creation of novel therapeutic agents.
Used in Medicinal Chemistry:
5-Methoxy-2-oxoindoline-3-carbaldehyde is employed as a key component in medicinal chemistry, where its unique molecular structure and reactivity are leveraged to design and synthesize potential pharmaceuticals.
Used in Biochemistry:
5-METHOXY-2-OXOINDOLINE-3-CARBALDEHYDE also finds applications in biochemistry, where it may be involved in the study of biological processes and the development of biochemical tools or agents.
Used in Material Science:
5-Methoxy-2-oxoindoline-3-carbaldehyde is used in material science for the development of new materials, taking advantage of its chemical properties to create innovative substances with specific characteristics.
Used in Agrochemicals Production:
Additionally, 5-Methoxy-2-oxoindoline-3-carbaldehyde plays a role as an intermediate in the production of various agrochemicals, contributing to the development of agricultural products and solutions.
Check Digit Verification of cas no
The CAS Registry Mumber 52508-88-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,5,0 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52508-88:
(7*5)+(6*2)+(5*5)+(4*0)+(3*8)+(2*8)+(1*8)=120
120 % 10 = 0
So 52508-88-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO3/c1-14-6-2-3-9-7(4-6)8(5-12)10(13)11-9/h2-5,8H,1H3,(H,11,13)
52508-88-0Relevant academic research and scientific papers
Oxindole alkaloids. A novel non-biomimetic entry to (-)-horsfiline
Palmisano, Giovanni,Annunziata, Rita,Papeo, Gianluca,Sisti, Massimo
, p. 1 - 4 (2007/10/03)
A novel non-biomimetic synthesis of horsfiline has been developed. The key pyrrolidine forming reaction is the 1,3-dipolar cycloaddition of the thermally generated N-methylazomethine ylide to a suitable 3-akylidene-indolin-2(3H)one. The same strategy was also applied to the synthesis of pure (R)-(-)-enantiomer.
