1100954-16-2

Basic information

• Product Name: CHEMBRDG-BB 4102529
• Synonyms: CHEMBRDG-BB 4102529;N-[(1-methyl-1H-pyrazol-4-yl)methyl]cyclopropanamine dihydrochloride;Cyclopropyl-(1-methyl-1H-pyrazol-4-ylmethyl)-amine
• CAS NO: 1100954-16-2
• Molecular Formula: C8H13N3
• Molecular Weight: 151.20892
• Mol File: 1100954-16-2.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: CHEMBRDG-BB 4102529(CAS DataBase Reference)
• NIST Chemistry Reference: CHEMBRDG-BB 4102529(1100954-16-2)
• EPA Substance Registry System: CHEMBRDG-BB 4102529(1100954-16-2)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 1100954-16-2(Hazardous Substances Data)

Upstream product

• 25016-11-9 1-methylpyrazole-4-carbaldehyde 

Relevant articles and documents

Triazole compound and application thereof in agriculture (by machine translation)

More specifically, the present invention relates to a; method for, preparing a triazole compound (I) represented by formula (I) or a salt (I) thereof, a salt thereof, and a method, for producing a, triazole compound, a salt thereof, and a method for controlling a, disease by using these compounds, and or compositions in the form of a fungicide and a; fungicide ,R composition thereof. 1 , R2 , Y, n, X, R3 , R4 The, m invention has Het .the meanings as described in the present invention. (by machine translation)

Design, Synthesis, and Biological Activity of Novel Triazole Sulfonamide Derivatives Containing a Benzylamine Moiety

The triazole sulfonamide played a very important role in the field of research of new agrochemical compounds as a novel heterocyclic compound with lack of reported resistance. For the research on the innovative triazole sulfonamide fungicide effective against cucumber downy mildew (CDM), the present article designed an array of 1,2,4-triazole-1,3-disulfonamide derivatives. The derivatives were synthesized via coupling multiple benzylamine with triazole sulfonamide groups. 1H-NMR, 13C-NMR, and LC–MS spectrometry were used to characterize these synthesized compounds. Most of these derivatives exhibited better fungicidal activities than that of the commercial cyanosole using bioassays. In particular, compounds 6g and 6h showed the best fungicidal activity against CDM (EC50?=?6.91 and 10.62?mg/L). Comparative experiments demonstrated that the fungicidal activity of 6g and 6h was better than the commercial pesticides amisulbrom and cyanosole. According to the study, the compound 6g had a giant application potential on fungicide against CDM.