111570-63-9 Usage
Description
(6E)-4-benzo[1,3]dioxol-5-yl-6-(2,4-dimethoxy-6-oxo-1-cyclohexa-2,4-dienylidene)-2,3a,4,5-tetrahydro-1H-indazol-3-one is a complex organic molecule characterized by a unique structure that includes a fused benzodioxole and cyclohexadienone ring system. (6E)-4-benzo[1,3]dioxol-5-yl-6-(2,4-dimethoxy-6-oxo-1-cyclohexa-2,4-di enylidene)-2,3a,4,5-tetrahydro-1H-indazol-3-one also features an indazole ring and two methoxy groups, which contribute to its potential pharmaceutical applications. The presence of heterocyclic rings and functional groups in its structure makes it a promising candidate for the development of anti-cancer, anti-inflammatory, or anti-viral drugs. Further research and studies are necessary to fully understand the properties and potential of this compound.
Uses
Used in Pharmaceutical Industry:
(6E)-4-benzo[1,3]dioxol-5-yl-6-(2,4-dimethoxy-6-oxo-1-cyclohexa-2,4-dienylidene)-2,3a,4,5-tetrahydro-1H-indazol-3-one is used as a potential candidate for drug development due to its unique structural features and the presence of heterocyclic rings and functional groups. Its potential applications include anti-cancer, anti-inflammatory, and anti-viral therapies.
Used in Research and Development:
In the field of scientific research, this compound serves as a valuable subject for further investigation. It is used as a test subject to study the effects of its structural features on biological activities and to explore its potential in the development of new pharmaceuticals.
Used in Drug Design and Synthesis:
(6E)-4-benzo[1,3]dioxol-5-yl-6-(2,4-dimethoxy-6-oxo-1-cyclohexa-2,4-dienylidene)-2,3a,4,5-tetrahydro-1H-indazol-3-one is utilized in drug design and synthesis processes to create new molecules with improved properties and enhanced therapeutic effects. Its unique structure and functional groups can be modified or combined with other molecules to develop novel drugs with specific target actions.
Used in Chemical Synthesis:
(6E)-4-benzo[1,3]dioxol-5-yl-6-(2,4-dimethoxy-6-oxo-1-cyclohexa-2,4-di enylidene)-2,3a,4,5-tetrahydro-1H-indazol-3-one can also be used as a starting material or intermediate in the synthesis of other complex organic molecules. Its unique structure and functional groups make it a valuable building block for the creation of new compounds with various applications in different industries, including pharmaceuticals, materials science, and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 111570-63-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,5,7 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 111570-63:
(8*1)+(7*1)+(6*1)+(5*5)+(4*7)+(3*0)+(2*6)+(1*3)=89
89 % 10 = 9
So 111570-63-9 is a valid CAS Registry Number.
InChI:InChI=1/C22H20N2O6/c1-27-13-8-16(25)20(19(9-13)28-2)12-5-14(21-15(6-12)23-24-22(21)26)11-3-4-17-18(7-11)30-10-29-17/h3-4,6-9,14,21,23H,5,10H2,1-2H3,(H,24,26)/b20-12-
111570-63-9Relevant articles and documents
Synthesis, Separation of Tautomers and Biological Activities of 4,6-Diaryl-3-oxo-3,3a,4,5-tetrahydro-2H-indazoles
Jain, A. C.,Mehta, A.,Arya, P.
, p. 150 - 153 (2007/10/02)
Three chalcones (1a, 1b and 1c) having phloroglucinol oxygenation pattern in ring-A have been converted into the corresponding 3,5-diaryl-6-carbethoxycyclohex-2-en-1-ones (2a, 2b and 2c) by the Michael condensation with ethyl acetoacetate in the presence
