29938-75-8

Upstream product

• 58011-00-0 (1,3-dimethyl-5-hydroxy-1H-pyrazol-4-yl)(3-chlorophenyl)methanone 
• 2749-59-9 1,3-dimethyl-5-pyrazolone 

Downstream Products

• 78451-73-7 4-(3-Chloro-phenyl)-1,3-dimethyl-6,6a,7,8,9,10-hexahydro-1H-1,2,5,10a-tetraaza-benzo[e]azulene 
• 51022-73-2 4-(3-chloro-phenyl)-1,3-dimethyl-1,6,7,8-tetrahydro-pyrazolo[3,4-e][1,4]diazepine 
• 54510-45-1 4-(3-chloro-phenyl)-1,3,6-trimethyl-1,6,7,8-tetrahydro-pyrazolo[3,4-e][1,4]diazepine 
• 54510-44-0 4-(3-chlorophenyl)-1,6,7,8-tetrahydro-1,3,8-trimethylpyrazolo<3,4-e><1,4>diazepine dihydrochloride 
• 54454-13-6 (5-amino-1,3-dimethyl-1H-pyrazol-4-yl)-(3-chloro-phenyl)-methanone 
• 78451-75-9 4-(3-chlorophenyl)-1,6,7,8-tetrahydro-3-methylpyrazolo[3,4-e][1,4]diazepine 
• 78451-74-8 4-(3-chlorophenyl)-1,6,7,8-tetrahydro-1,3-dimethylpyrazolo[3,4-e][1,4]diazepine 5-oxide 
• 78451-69-1 4-(3-chlorophenyl)-1,6,7,8-tetrahydro-1,3-dimethyl-8-nitrosopyrazolo[3,4-e][1,4]diazepine 
• 78451-70-4 {3-[4-(3-Chloro-phenyl)-1,3-dimethyl-6,7-dihydro-1H-pyrazolo[3,4-e][1,4]diazepin-8-yl]-propyl}-dimethyl-amine 
• 78451-98-6 4-(3-chlorophenyl)-8-(trifluoroacetyl)-1,6,7,8-tetrahydro-1,3-dimethylpyrazolo<3,4-e><1,4>diazepine 
• 54454-18-1 8-acetyl-4-(3-chlorophenyl)-1,6,7,8-tetrahydro-1,3-dimethylpyrazolo<3,4-e><1,4>diazepine hydrochloride 
• 1581307-13-2 (3-chlorophenyl)(1,3-dimethyl-5-(phenylthio)-1H-pyrazol-4-yl)methanone 
• 1581307-14-3 (3-chlorophenyl)(5-(4-chlorophenylthio)-1,3-dimethyl-1H-pyrazol-4-yl)methanone 
• 1581307-15-4 (3-chlorophenyl)(5-(4-isopropylphenylthio)-1,3-dimethyl-1H-pyrazol-4-yl)methanone 

Relevant academic research and scientific papers

The synthesis and biological activities of [5-(4-substituted phenylsulfinyl/sulfonyl)-1,3-dimethyl-1 H-pyrazol-4-Yl]-arylmethanones

A novel series of pyrazole derivatives containing substituted phenylsulfinyl/sulfonyl group have been synthesized via the oxidation of intermediate pyrazole sulfoether with H2O2 in acetic acid. The novel compounds were characterized by melting point, 1H NMR, FT-IR, MS, and elemental analysis or HRMS. The biological activity results showed that most of the title compounds exhibit significant fungicidal activities against Alternaria solani Sorauer, Phytophthora capsici, and Corynespora cassiicola. [Supplementary materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements for the following free supplemental files: Additional text and figures.]