116170-84-4

Usage

InChI:InChI=1/C9H9NO2S2/c1-3-12-8(11)7-4-6(5-10)9(13-2)14-7/h4H,3H2,1-2H3

Upstream product

• 116170-90-2 3-amino-4-cyano-5-(methylthio)thiophene-2-carboxylic acid ethyl ester 
• 5147-80-8 [Bis(methylthio)methylene]malononitrile 

Downstream Products

• 909252-76-2 tert-butyl 5-(N'-methyl-N'-phenylhydrazinocarbonyl)-3-[4-(4-methylpiperazin-1-ylmethyl)benzoylamino]-thieno[2,3-c]pyrazole-1-carboxylate 
• 909253-00-5 tert-butyl 5-(N'-methyl-N'-phenylhydrazinocarbonyl)-3-[3-(4-methylpiperazin-1-ylmethyl)-benzoylamino]thieno[2,3-c]pyrazole-1-carboxylate 
• 909252-68-2 tert-butyl 5-(N'-methyl-N'-phenylhydrazinocarbonyl)-3-(4-morpholin-4-ylmethylbenzoylamino)thieno[2,3-c]pyrazole-1-carboxylate 
• 909252-75-1 N-[5-(N'-methyl-N'-phenylhydrazinocarbonyl)-1H-thieno[2,3-c]pyrazol-3-yl]-4-(4-methylpiperazin-1-ylmethyl)benzamide 
• 909252-67-1 N-[5-(N'-methyl-N'-phenylhydrazinocarbonyl)-1H-thieno[2,3-c]pyrazol-3-yl]-4-morpholin-4-ylmethylbenzamide 
• 909252-74-0 tert-butyl 3-(4-bromobenzoylamino)-5-(N'-methyl-N'-phenylhydrazinocarbonyl)thieno[2,3-c]pyrazole-1-carboxylate 
• 909252-73-9 4-bromo-N-[5-(N'-methyl-N'-phenylhydrazinocarbonyl)-1H-thieno[2,3-c]pyrazol-3-yl]benzamide 
• 909252-69-3 tert-butyl 3-amino-5-(N'-methyl-N'-phenylhydrazinocarbonyl)-thieno[2,3-c]pyrazole-1-carboxylate 
• 909252-70-6 N'-methyl-N'-phenyl(3-amino-1H-thieno[2,3-c]pyrazole)-5-carbohydrazide 
• 909252-83-1 N'-methyl-N'-phenyl(4-cyano-5-methanesulfinylthiophene)-2-carbohydrazide 
• 909252-84-2 N'-methyl-N'-phenyl(4-cyano-5-methanesulfonylthiophene)-2-carbohydrazide 
• 909252-85-3 N'-(4-chlorophenyl)-N'-methyl(4-cyano-5-methanesulfinylthiophene)-2-carbohydrazide 
• 909252-86-4 N'-(4-chlorophenyl)-N'-methyl(4-cyano-5-methanesulfonylthiophene)-2-carbohydrazide 
• 116170-85-5 4-cyano-5-(methylthio)thiophene-2-carboxylic acid 

Relevant academic research and scientific papers

Hydrazinocarbonyl-thieno[2,3-C]pyrazoles, Process for Preparing Them, Compositions Containing Them and Use Thereof

The present invention concerns hydrazinocarbonyl-thieno[2,3-c]pyrazoles of formula (I): wherein R1, R3, R4, are R5 are as defined in the disclosure; their preparation method, compositions containing the same and their use for the treatment of pathological conditions, in particular as anticancer agents.

Thio compounds having fungicidal activity

The invention relates to new thio compounds of the general formula STR1 wherein R is an alkyl group substituted or not substituted with halogen and having 1-12 carbon atoms, an alkenyl or alkynyl group having 2-4 carbon atoms, an alkadienyl group having 3 or 4 carbon atoms or a substituted or unsubstituted phenyl or phenyl(C1 -C4)alkyl group; R1 is a cyano group, a formyl group, an alkylcarbonyl or alkoxycarbonyl group substituted or unsubstituted with halogen and having 2-5 carbon atoms, a substituted or unsubstituted benzoyl group, or an alkylsulphonyl group having 1-4 carbon atoms; R2 is a hydrogen atom, a halogen atom, an amino group unsubstituted or substituted with one or two groups selected from C1 -C4 alkyl and C2 -C5 alkylcarbonyl, an amino group forming part of a heterocyclic ring which may comprise 1 or 2 additional heteroatoms selected from N, O and S, an alkyl or alkoxy group having 1-4 carbon atoms and optionally substituted with C2 -C5 alkylcarbonyl, or a substituted or unsubstituted phenyl, phenoxy or phenylthio group; or wherein R1 and R2, together with the vinylene group to which they are bound, constitute a substituted or unsubstituted phenyl group; X is a cyano group or a formyl group; n is 1 or 2; Y is an alkylthio group having 1-4 carbon atoms; and Z is a hydrogen atom, a halogen atom, a nitro group, or an alkyl or alkoxy group having 1-4 carbon atoms and optionally substituted with halogen; or wherein Y and Z together constitute a sulphur atom; with the proviso that, when Y and Z do not together constitute a sulphur atom, R1 and R2, together with the vinylene group to which they are bound, constitute a substituted or unsubstituted phenyl group. The new compounds show a fungicidal and/or bactericidal activity and may be used in particular against plantpathogenic seed fungi and soil fungi and/or bacteria.