25629-58-7 Usage
Uses
Used in Pharmaceutical Research and Development:
5-chloro-3-hydroxyisothiazole is used as a synthetic intermediate for the development of complex organic compounds, particularly in the pharmaceutical industry. Its unique structure allows for the creation of new drugs with potential therapeutic applications.
Used in Agrochemical Research and Development:
5-chloro-3-hydroxyisothiazole is used as a building block in the synthesis of agrochemicals, such as pesticides and herbicides. Its chemical properties enable the design of novel compounds that can be more effective and environmentally friendly.
Used in Chemical Synthesis:
5-chloro-3-hydroxyisothiazole is used as a reagent in various chemical reactions, allowing for the formation of a wide range of organic compounds. Its versatility in synthesis makes it a valuable tool in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 25629-58-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,6,2 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 25629-58:
(7*2)+(6*5)+(5*6)+(4*2)+(3*9)+(2*5)+(1*8)=127
127 % 10 = 7
So 25629-58-7 is a valid CAS Registry Number.
25629-58-7Relevant academic research and scientific papers
Synthesis and antibacterial activity of 2-(4-substituted phenyl)-3(2H)-isothiazolones
Khalaj, Ali,Adibpour, Neda,Shahverdi, Ahmad Reza,Daneshtalab, Mohsen
, p. 699 - 705 (2007/10/03)
Several new and known 2-(4-substituted phenyl)-3(2H)-isothiazolone derivatives with or without chloro substituent at C-5 position were synthesized and their in vitro antibacterial activity against selected Gram-negative and Gram-positive bacteria were eva
A General Synthesis of N-Substituted Isothiazol-3(2H)-ones
Beeley, Nigel R. A.,Harwood, Laurence M.,Hedger, Paul C.
, p. 2245 - 2252 (2007/10/02)
A general route to the synthesis of N-substituted isothiazol-3(2H)-ones (4a-i) is described which proceeds via trichloroacetic acid-mediated ring closure of N-substituted (Z)-3-(benzylsulfinyl)propenamides (15a-i).
