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.
This compound 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 articles and documents
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.
