88166-78-3

Upstream product

• 2142-73-6 1-(2,5-dimethylphenyl)-1-ethanone 

Downstream Products

• 2142-73-6 1-(2,5-dimethylphenyl)-1-ethanone 
• 129993-24-4 N-vinyl-2-(2,5-dimethylphenyl)pyrrole 
• 132907-21-2 2-(2,5-Dimethylphenyl)pyrrole 
• 142426-02-6 O-vinyl-2,5-dimethylacetophenone oxime 
• 95-78-3 2,5-Dimethylaniline 
• 1333120-03-8 2,6-bis(2,5-dimethylphenyl)-4-phenylpyridine 
• 1333119-98-4 C₁₂H₁₅NO₂ 
• 1392763-61-9 C₁₈H₁₉NO₄ 
• 1268140-64-2 C₁₂H₁₃NO 
• 886-66-8 1,4-diphenyl-1,3-butadiyne 
• 1260236-31-4 N-[1-(2,5-dimethylphenyl)vinyl]acetamide 
• 1604842-42-3 C₁₈H₂₁NO₄ 

Relevant academic research and scientific papers

Synthesis of Functionalized Vinylsilanes via Metal-Free Dehydrogenative Silylation of Enamides

A novel method of metal-free dehydrogenative silylation of enamides has been developed. The desired functionalized vinylsilane products were obtained in moderate to good yield and with high stereoselectivities. This protocol displays good tolerance of various functionalities. Furthermore, the high chemoselectivity of this reaction enables us to introduce different unsaturated C-C moieties to the products. The ease of further derivatization of the products to other useful compounds also demonstrates the highly synthetic utility of the current methodology.

TETRAZOLINONE COMPOUND AND USE THEREOF

The compound represented by formula (1): wherein R4 and R5 each represents a hydrogen atom, a halogen atom, or a C1-C3 alkyl group; R6 represents a C1-C4 alkyl group, a C3-C6 cycloalkyl group, or the like; R7, R8, and R9 each represents a hydrogen atom, a halogen atom, or the like; R10 represents a C1-C3 alkyl group, or the like; R13 represents a C1-C3 alkyl group, or the like; and Q represents a phenyl group, or the like; has an excellent control effect on pests.