7272-58-4 Usage
Uses
Used in Pharmaceutical Research:
4,5,6,7-tetrahydro-3-methyl-4-oxo-indole-2-carboxylicaciethylester is used as a building block for the creation of new drugs in pharmaceutical research. Its diverse range of biological activities, including antibacterial, antifungal, and antiviral properties, make it a valuable component in the development of medications for various infections.
Used in Antibacterial Applications:
4,5,6,7-tetrahydro-3-methyl-4-oxo-indole-2-carboxylicaciethylester is used as an antibacterial agent in the development of medications for treating bacterial infections. Its ability to inhibit bacterial growth makes it a promising candidate for combating antibiotic-resistant strains.
Used in Antifungal Applications:
4,5,6,7-tetrahydro-3-methyl-4-oxo-indole-2-carboxylicaciethylester is used as an antifungal agent in the development of medications for treating fungal infections. Its potential to inhibit fungal growth and prevent the spread of infections makes it a valuable component in antifungal drug discovery.
Used in Antiviral Applications:
4,5,6,7-tetrahydro-3-methyl-4-oxo-indole-2-carboxylicaciethylester is used as an antiviral agent in the development of medications for treating viral infections. Its ability to inhibit viral replication and reduce the severity of viral diseases makes it a promising candidate for antiviral drug development.
Used in Anti-inflammatory and Analgesic Applications:
4,5,6,7-tetrahydro-3-methyl-4-oxo-indole-2-carboxylicaciethylester is used as an anti-inflammatory and analgesic agent in the development of medications for treating inflammation and pain. Its potential to reduce inflammation and alleviate pain makes it a valuable component in the field of drug discovery and development.
Overall, 4,5,6,7-tetrahydro-3-methyl-4-oxo-indole-2-carboxylicaciethylester holds promise for its therapeutic applications and continues to be a subject of interest in scientific research, particularly in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 7272-58-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,7 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7272-58:
(6*7)+(5*2)+(4*7)+(3*2)+(2*5)+(1*8)=104
104 % 10 = 4
So 7272-58-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO3/c1-3-16-12(15)11-7(2)10-8(13-11)5-4-6-9(10)14/h13H,3-6H2,1-2H3
7272-58-4Relevant academic research and scientific papers
Thiopyrano[2,3-e]indol-2-ones: Angelicin heteroanalogues with potent photoantiproliferative activity
Barraja, Paola,Diana, Patrizia,Montalbano, Alessandra,Carbone, Anna,Cirrincione, Girolamo,Viola, Giampietro,Salvador, Alessia,Vedaldi, Daniela,Dall'Acqua, Francesco
experimental part, p. 9668 - 9683 (2009/04/06)
A new class of compounds, the thiopyrano[2,3-e]indol-2-ones, bioisosters of the angular furocoumarin angelicin, was synthesized with the aim of obtaining new photochemotherapeutic agents. In particular 7,8-dimethyl-thiopyranoindolone 6c s showed a remarka
The intramolecular photometathesis of pyrroles
Elliott, Luke D.,Berry, Malcolm,Orr-Ewing, Andrew J.,Booker-Milburn, Kevin I.
, p. 3078 - 3079 (2007/10/03)
UV irradiation of various electron deficient pyrrole derivatives induces a novel methathesis sequence resulting in selective cleavage of the 2,3-pyrrole bond. The overall sequence has been shown to proceed by two discrete wavelength-dependent steps involving sequential [2+2] cyclobutane formation followed by photochemically mediated retro-[2+2] to the products. Copyright
Synthesis of ethyl pyrrole-2-carboxylates: A regioselective cyclization of enaminones under knorr-type conditions
Elghamry, Ibrahim
, p. 897 - 902 (2007/10/03)
A regioselective formation of ethyl pyrrole-2-carboxylates 4 and 5 is effected by reductive condensation of enaminones 1a-f and ethyl 2-oximinoacetoacetate 2. The structures of the products have been delineated by spectroscopic methods.
Porphyrins with Exocyclic Rings. 1. Chemistry of 4,5,6,7-Tetrahydro-1H-indoles: Synthesis of Acetoxy Derivatives, Dihydroindoles, and Novel Porphyrins with Four Exocyclic Rings
Lash, Timothy D.,Bladel, Karla A.,Shiner, Craig M.,Zajeski, Donna L.,Balasubramaniam, Rajiv P.
, p. 4809 - 4820 (2007/10/02)
A variety of 4,5,6,7-tetrahydro-1H-indoles (THI's) and 4-oxo-4,5,6,7-tetrahydro-1-indoles (4-oxoTHI's) have been synthesized from cyclohexanone and 1,3-cyclohexanedione, respectively.The THI's reacted regioselectively with lead tetraacetate in acetic acid
Photochemical Heterocyclization of Functionalized Dienamines
Gelas-Mialhe, Yvonne,Mabiala, Gaston,Vessiere, Roger
, p. 5395 - 5400 (2007/10/02)
A series of functionalized dienamines were prepared by base-catalyzed isomerisation of N-vinylaziridines.Photochemical cyclization of these N-substituted dienamines yielded predominantly pyrroline derivatives.
