4702-25-4 Usage
Uses
Used in Organic Synthesis:
Isoquinolin-1-thione is used as a reagent in organic synthesis for the preparation of various compounds. Its unique structure allows for versatile chemical reactions, making it a valuable component in the synthesis of a wide range of organic molecules.
Used in Pharmaceutical Research:
Isoquinolin-1-thione is utilized in pharmaceutical research as a potential drug candidate. Its biological activities, such as antibacterial, antifungal, and antiviral properties, make it a promising candidate for the development of new therapeutic agents to combat various diseases.
Used in Agrochemical Production:
Isoquinolin-1-thione is employed in the production of agrochemicals. Its chemical properties and potential biological activities contribute to the development of effective agricultural products, such as pesticides and herbicides, to protect crops and enhance agricultural productivity.
Used in Materials Science and Organic Electronics:
Isoquinolin-1-thione may have potential applications in the fields of materials science and organic electronics. Its unique structure and properties could be harnessed to develop new materials with specific characteristics, such as improved conductivity or enhanced stability, for use in electronic devices and other applications.
Check Digit Verification of cas no
The CAS Registry Mumber 4702-25-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,0 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4702-25:
(6*4)+(5*7)+(4*0)+(3*2)+(2*2)+(1*5)=74
74 % 10 = 4
So 4702-25-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H7NS/c11-9-8-4-2-1-3-7(8)5-6-10-9/h1-6H,(H,10,11)
4702-25-4Relevant academic research and scientific papers
ELECTRON DEFICIENT HETEROAROMATIC AMMONIOAMIDATES, XVIII. THE SYNTHESIS AND PHOTOCHEMISTRY OF SOME N-ISOQUINOLINO(THIOAMIDATES)
Lempert-Sreter, M.,Lempert, K.,Tamas, J.,Vekey, K.
, p. 259 - 270 (2007/10/02)
Thioacylation of isoquinolinioamide furnished the N-isoquinolinio(thioamidates) 2a-2c.Depending on the solvent, 2c exists either as a mixture with its tricyclic tautomer 5, or exclusively as the latter.The NMR and mass spectra, and the photochemistry of compounds 2a-2c are discussed.The photoproducts obtained include 3,4-dimethoxybenzonitrile, 3,4-dimethoxy(thiobenzamide), O-ethyl thiocarbamate, 1(2H)-isoquinolinethione (7a), 1(2H)-isoquinolinone (7b) and thiadiazoloisoquinolin-4-ium-2-olate (8a).Differences between the fragmentation upon electron impact and the photochemistry of the thioamidates of Types 1 and 2, as well as between the photochemistry of the thioamidates 2 and their amidate counterparts of Type 3 are discussed.Potassium permanganate oxidation of thiadiazoloisoquinolin-4-ium-2-thiolate (8b) furnishes the olate 8a and 1-isoquinolyl thiocyanate (12).
