141622-83-5 Usage
Properties
1. Chemical Structure: Methyl ester derivative of 3-Isoquinolinecarboxylic acid.
2. Biological Activities: Demonstrates anti-inflammatory and anti-cancer properties.
3. Therapeutic Potential: Investigated for its potential in treating various conditions such as cancer, inflammation, and neurological disorders.
4. Molecular Structure: Contains a tetrahydro-1,4-dioxo moiety and a phenylmethoxy substituent.
Specific Content
1. Chemical Name: 3-Isoquinolinecarboxylic acid, 1,2,3,4-tetrahydro-1,4-dioxo-3-(phenylmethoxy)-, methyl ester.
2. Biological Activities: Anti-inflammatory and anti-cancer properties.
3. Research Focus: Investigated for therapeutic potential in cancer, inflammation, and neurological disorders.
4. Molecular Structure: Contains a methyl ester group, a tetrahydro-1,4-dioxo moiety, and a phenylmethoxy substituent.
5. Medicinal Chemistry: Considered a promising candidate for further study and development due to its molecular structure and properties.
3-Isoquinolinecarboxylic acid,
1,2,3,4-tetrahydro-1,4-dioxo-3-(phenylmethoxy)-, methyl ester holds promise for pharmaceutical applications due to its diverse biological activities and molecular structure, making it a subject of interest in medicinal chemistry research.
Check Digit Verification of cas no
The CAS Registry Mumber 141622-83-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,6,2 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 141622-83:
(8*1)+(7*4)+(6*1)+(5*6)+(4*2)+(3*2)+(2*8)+(1*3)=105
105 % 10 = 5
So 141622-83-5 is a valid CAS Registry Number.
141622-83-5Relevant academic research and scientific papers
Unusual Oxidation in Thionyl Chloride: Novel Synthesis of Methyl 3-alkoxy-1,4-dioxo-1,2,3,4-tetrahydroisoquinoline-3-carboxylates
Beattie, John F.,Hales, Neil J.
, p. 751 - 752 (2007/10/02)
Oxidation of methyl 1,4-dioxo-1,2,3,4-tetrahydroisoquinoline-3-carboxylate 1 with thionyl chloride gives an unstable intermediate that reacts with alcohols to give 3-alkoxy-1,4-dioxo-1,2,3,4-tetrahydroisoquinoline-3-carboxylates (e.g. 6) and that is reduced with N-acetylcysteine to regenerate 1.In this system thionyl chloride is a convenient alternative oxidant to lead tetraacetate for the preparation of these masked equivalents of the unusual and reactive dienophile methyl 1,4-dioxo-1,4-dihydroisoquinoline-3-carboxylate 7.
