927-63-9Relevant articles and documents
A process for preparing pirazole carbaldehyde compounds
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Paragraph 0069-0077, (2018/02/24)
The present invention relates to a method for preparing pirazole carbaldehyde compounds and, more specifically, to a novel method for preparing 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carbaldehyde and 3-(trifluoromethyl)-1-methyl-1-H-pyrazole-4-carbaldehyde which are useful as intermediates for producing pyrazole carboxanilide disinfectants such as isopyrazam, sedaxane, bixafen, etc. According to the present invention, production costs of pyrazole carboxanilide disinfectants can be reduced.COPYRIGHT KIPO 2017
Computer aided benzothiazole derivatives. Synthesis, structure and biological study of new push-pull conjugated benzothiazolium salts
Buffa,Zahradnik,Foltinova
, p. 331 - 336 (2007/10/03)
As the conjugation is assumed to enhance the biological activity of push-pull type benzothiazolium salts, new compounds with extended conjugated bridge between benzothiazolium and phenyl ring were designed and synthesized. The compounds have been tested against the model microorganism Euglena gracilis as well as 6 microorganisms including Gram-positive and Gram-negative bacteria , a yeast and a mould. In accordance with predictions, the prepared compounds showed enhanced activity against Euglena and Gram-positive bacteria and some of them also interesting fungicidal and fungistatic activity.
REACTION OF AMINALS OF CONJUGATED ω-DIMETHYLAMINO ALDEHYDES WITH INDANEDIONE
Krasnaya, Zh. A.,Stytsenko, T. S.,Gusev, D. G.,Prokof'ev, E. P.
, p. 1446 - 1452 (2007/10/02)
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