3326-88-3 Usage
Uses
Used in Pharmaceutical Industry:
3H-1,2-Dithiol-3-one is used as an antibiotic agent for its ability to combat various bacterial infections. Its unique structure allows it to interact with biological systems, making it a promising candidate for the development of new antimicrobial drugs.
Used in Agricultural Industry:
In agriculture, 3H-1,2-Dithiol-3-one is utilized as a biocidal agent to protect crops from harmful pathogens and pests. Its antibiotic properties help in maintaining the health of the plants and improving overall crop yield.
Used in Organic Synthesis:
3H-1,2-Dithiol-3-one serves as a key intermediate in the synthesis of various organic compounds. Its reactive sulfur atoms facilitate multiple chemical reactions, making it a valuable component in the creation of complex organic molecules.
Used in Material Science:
3H-1,2-Dithiol-3-one is employed in material science for the development of new materials with unique properties. Its incorporation into polymers and other materials can enhance their stability, reactivity, or other characteristics, contributing to advances in material technology.
The diverse applications of 3H-1,2-Dithiol-3-one underscore its versatility and potential for further research and development across multiple disciplines.
Check Digit Verification of cas no
The CAS Registry Mumber 3326-88-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,2 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3326-88:
(6*3)+(5*3)+(4*2)+(3*6)+(2*8)+(1*8)=83
83 % 10 = 3
So 3326-88-3 is a valid CAS Registry Number.
3326-88-3Relevant academic research and scientific papers
HIGH-TEMPERATURE ORGANIC SYNTHESIS XLIII. REACTIONS OF ORGANIC DISELENIDES WITH PROPARGYL ALCOHOL
Deryagina, E. N.,Korchevin, N. A.,Voronkov, M. G.
, p. 1069 - 1072 (2007/10/02)
The gas-phase reaction of propargyl alcohol with dialkyl diselenides at 400 - 430 deg C leads to a high yield of 1,2-diselenol-3-one. 1,2-Diselenol-3-one is formed in a similar way from diphenyl diselenide at 450 - 500 deg C but with a low yield.The mechanism of the thermal dissociation of the diselenides and their reactions with propargyl alcohol is discussed.
