40994-01-2

Upstream product

• 5333-86-8 ethyl benzimidate hydrochloride 
• 60-34-4 methylhydrazine 
• 1670-14-0 benzamidine monohydrochloride 
• 22038-72-8 methyldiazene 
• 7471-86-5 methyl benzimidate 

Downstream Products

• 52713-97-0 2-methyl-5-phenyl-2H-1,2,4,3-triazaphosphole 
• 75955-00-9 4,5-dihydro-1,5,5-trimethyl-3-phenyl-1H-1,2,4-triazole 
• 39696-58-7 1-methyl-3-phenyl-1H-1,2,4-triazole 
• 68301-11-1 1,5-dimethyl-3-phenyl-1H-1,2,4-triazole 
• 75373-26-1 Dimethyl-(1-methyl-3-phenyl-6,9-dithia-1,2,4-triaza-5λ⁵-phospha-spiro[4.4]non-2-en-5-yl)-amine 

Relevant academic research and scientific papers

Olefination via Cu-Mediated Dehydroacylation of Unstrained Ketones

The dehydroacylation of ketones to olefins is realized under mild conditions, which exhibits a unique reaction pathway involving aromatization-driven C-C cleavage to remove the acyl moiety, followed by Cu-mediated oxidative elimination to form an alkene between the α and β carbons. The newly adopted N′-methylpicolinohydrazonamide (MPHA) reagent is key to enable efficient cleavage of ketone C-C bonds at room temperature. Diverse alkyl- and aryl-substituted olefins, dienes, and special alkenes are generated with broad functional group tolerance. Strategic applications of this method are also demonstrated.

NOVEL OXABOROLE ANALOGS AND USES THEREOF

This application describes compounds, compositions, and methods which are useful in treating, preventing, inhibiting, ameliorating, or eradicating the pathology and/or symptomology of a disease caused by a parasite.

STRUCTURE OF THE PRODUCTS FROM CONDENSATION OF AMIDRAZONES WITH MONOCARBONYL COMPOUNDS

The structure of the products from the reaction of amidrazones with monocarbonyl compounds was invwstigated by spectral methods (IR, UV, (1)H and (13)C NMR). 1-Monosubstituted acetamidrazones and benzamidrazones form 1,3,5,5-tetrasubstituted 4,5-dihydro-1,2,4-triazoles, and the unsubstituted amidrazones form alkylidyne derivatives.