53599-13-6 Usage
Uses
Used in Pharmaceutical Research:
2,3-Dihydro-2-hydroxyiminobenzo[b]thiophen-3-one is utilized as a research compound for exploring its potential biological activities and therapeutic applications. Its unique structure suggests it may interact with biological targets in novel ways, offering opportunities for the development of new drugs.
Used in Drug Development:
In the drug development industry, 2,3-Dihydro-2-hydroxyiminobenzo[b]thiophen-3-one is used as a lead compound for the design and synthesis of new pharmaceutical agents. Its chemical properties and potential interactions with biological systems make it a candidate for further investigation to understand its full potential in treating various diseases.
Further studies are necessary to elucidate the properties and potential uses of 2,3-Dihydro-2-hydroxyiminobenzo[b]thiophen-3-one, as its current applications are primarily confined to research and development settings. As our understanding of 2,3-Dihydro-2-hydroxyiminobenzo[b]thiophen-3-one grows, it may find broader applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 53599-13-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,9 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 53599-13:
(7*5)+(6*3)+(5*5)+(4*9)+(3*9)+(2*1)+(1*3)=146
146 % 10 = 6
So 53599-13-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H5NO2S/c10-7-5-3-1-2-4-6(5)12-8(7)9-11/h1-4,11H/b9-8+
53599-13-6Relevant academic research and scientific papers
Nakazumi,Endo,Nakaue,Kitao
, p. 89 - 92 (1985)
3-Amino-4H-1-benzothiopyran-4-one (3-aminothiochromone) was easily prepared by reaction of 3-bromothiochromen-4-one with sodium azide in methanol-water. Condensation of 3-aminothiochromone with diethyl ethoxymethylenemalonate and with dimethyl acetylenedicarboxylate gave intermediates, which were thermally cyclized to give 4,10-dihydro-4,10-doxo-1H[1]benzothiopyrano[3,2-b]pyridinecarboxylates. 3-Formyl-thiochromone was condensed with o-phenylenediamine to give 7-oxo-7,13-dihydro[1]benzothiopyrano[2,3-b]-1,5-benzodiazepine.