30707-68-7 Usage
Uses
Used in Pharmaceutical Industry:
1-(2',4',6'-Trichlorophenyl)-3-(2'-chloro-5'-nitroanilino)-5-pyrazolone is used as a potential pharmaceutical compound for its possible biological activity. The exact application reason is not specified due to limited information, but its structure suggests it could be involved in drug development.
Used in Agrochemical Industry:
1-(2',4',6'-Trichlorophenyl)-3-(2'-chloro-5'-nitroanilino)-5-pyrazolone is used as a potential agrochemical compound for its possible biological activity. The exact application reason is not specified due to limited information, but its structure suggests it could be involved in the development of pesticides or other agricultural chemicals.
Note: Due to the lack of detailed information on the exact properties, toxicity, and applications of 1-(2',4',6'-Trichlorophenyl)-3-(2'-chloro-5'-nitroanilino)-5-pyrazolone, the above uses are speculative and based on the compound's structural features. Further research and testing would be required to confirm its suitability for these applications.
Check Digit Verification of cas no
The CAS Registry Mumber 30707-68-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,7,0 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 30707-68:
(7*3)+(6*0)+(5*7)+(4*0)+(3*7)+(2*6)+(1*8)=97
97 % 10 = 7
So 30707-68-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H8Cl4N4O3/c16-7-3-10(18)15(11(19)4-7)22-14(24)6-13(21-22)20-12-5-8(23(25)26)1-2-9(12)17/h1-5H,6H2,(H,20,21)
30707-68-7Relevant academic research and scientific papers
Synthesis of 3-(2-Chloro-5-nitroanilino and 4-nitroanilino)-1-(2,4,6-trichlorophenyl)-2-pyrazolin-5-ones
Kim, Chang-Kyu,Debellis, Francesco,Maggiulli, Cataldo A.
, p. 325 - 328 (2007/10/02)
A new synthesis of 3-anilino-1-aryl-2-pyrazolin-5-ones in which the pyrazolinone ring is built via N-N bond formation is described. 2-Cyano-2',4',6'-trichloroacetanilide 1 was converted to imino ether hydrochloride 2 which was reacted with anilines in methanol to produce N-arylimino ether 3a,b.Reaction of these N-arylimino ethers with hydroxylamine gave N-arylamidoximes 4a,b.An 1,2,4-oxadiazol-5-one 6a was prepared from the N-arylamidoxime 4a and subjected to base-induced rearrangement.The desired 3-anilinopyrazolinone 7a was obtained only in a very low yield.However, O-acetylation of the N-arylamidoximes 4a,b followed by acid-catalyzed ring closure and rearrangement in the presence of excess acetic anhydride gave a mixture of N-acetylanilinopyrazolinones (e.g. 10) and 4-acetyloxy-3-N-acetylanilinopyrazoles (e.g. 12) which upon acid hydrolysis afforded the 3-anilinopyrazolinones 7a,b in better yield.
Method for preparing 1-aryl-3-arylamino-2-pyrazolin-5-ones from N-aryl-3-arylamino-3-oximinopropionamides
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, (2008/06/13)
A method for preparing a 1-aryl-3-arylamino-2-pyrazolin-5-one comprises reacting an N-aryl-3-arylamino-3-oximinopropionamide with an acylating agent in an inert solvent, then heating in contact with a strong acid catalyst and a dehydrating agent in an inert solvent, and then heating in contact with an acid in water and a lower alkanol.
