73816-46-3 Usage
Uses
Used in Pharmaceutical Industry:
5,6-Dimethylisatin is used as a precursor for the synthesis of various pharmaceutical compounds due to its unique chemical structure and properties.
Used in Chemical Industry:
5,6-Dimethylisatin is used as a precursor in the synthesis of dyes, taking advantage of its yellow crystalline nature and chemical reactivity.
Used in Enzyme Inhibition:
5,6-Dimethylisatin is used as an inhibitor of the enzyme tyrosine hydroxylase, which plays a crucial role in the synthesis of dopamine. This application is significant in the study and treatment of neurological disorders related to dopamine imbalances.
Used in Antibacterial Applications:
5,6-Dimethylisatin has been investigated for its potential antibacterial activities, making it a candidate for development as an antimicrobial agent in various applications, such as in healthcare or consumer products.
Used in Antifungal Applications:
5,6-Dimethylisatin has also been studied for its potential antifungal properties, indicating its possible use in treating fungal infections or as a component in antifungal products.
Check Digit Verification of cas no
The CAS Registry Mumber 73816-46-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,1 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73816-46:
(7*7)+(6*3)+(5*8)+(4*1)+(3*6)+(2*4)+(1*6)=143
143 % 10 = 3
So 73816-46-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO2/c1-5-3-7-8(4-6(5)2)11-10(13)9(7)12/h3-4H,1-2H3,(H,11,12,13)
73816-46-3Relevant academic research and scientific papers
Combinatorial optimization of isatin-β-thiosemicarbazones as anti-poxvirus agents
Pirrung, Michael C.,Pansare, Sunil V.,Das Sarma, Koushik,Keith, Kathy A.,Kern, Earl R.
, p. 3045 - 3050 (2007/10/03)
Novel strategies are required to combat pox virus infections, whether caused by escape of viruses such as monkeypox from indigenous areas or intentional release of smallpox. Anti-smallpox drugs with a unique mode of antiviral action, inhibition of transcription termination, were known but not therapeutically useful. Using a combinatorial method, variants of the basic isatin-β-thiosemicarbazone structure were prepared and examined for cytotoxicity and antiviral activity in vaccinia virus- and cowpox virus-infected human cells. Potent and much more selective N-aminomethyl-isatin-β- thiosemicarbazones were discovered.
