36776-29-1

Upstream product

• 99-54-7 3,4-dichloronitrobenzene 
• 29682-39-1 1-bromo-2-chloro-4-nitrobenzene 
• 305-40-8 N-Acetyl-S-(2-chlor-4-nitro-phenyl)-L-cystein 

Downstream Products

• 203251-40-5 1-(4-tert-Butyl-phenyl)-2-(2-chloro-4-nitro-phenylsulfanyl)-ethanone 
• 209911-00-2 2-(2-Chloro-4-nitro-phenylsulfanyl)-1-thiophen-2-yl-ethanone 
• 15178-53-7 4-mercapto-3-chloroaniline 
• 203251-44-9 1-(3-Chloro-4-fluoro-phenyl)-2-(2-chloro-4-nitro-benzenesulfonyl)-ethanone 
• 209911-01-3 2-(2-Chloro-4-nitro-benzenesulfonyl)-1-thiophen-2-yl-ethanone 
• 315227-28-2 C₁₃H₆Cl₂N₂O₂S₂ 
• 203251-39-2 2-(2-Chloro-4-nitro-phenylsulfanyl)-1-(4-methoxy-phenyl)-ethanone 
• 203251-38-1 2-(2-Chloro-4-nitro-phenylsulfanyl)-1-(4-fluoro-phenyl)-ethanone 
• 203251-41-6 1-(3-Chloro-4-fluoro-phenyl)-2-(2-chloro-4-nitro-phenylsulfanyl)-ethanone 
• 20201-04-1 1,2-bis(2-chloro-4-nitrophenyl)disulfane 

Relevant academic research and scientific papers

BENZAZEPINE DERIVATIVE, PROCESS FOR PRODUCING THE SAME, AND USE

The present invention provides a novel benzazepine derivative represented by formula : wherein, R1 is a 5- or 6-membered aromatic ring, R2 is lower alkyl group, etc., Y is an optionally substituted imino group, ring A and ring B are independently an optionally substituted aromatic ring, W is formula -W1-X2-W2- (W1 and W2 are independently S(O)m1 (m1 is 0, 1 or 2), etc., and X2 is an optionally substituted alkylene groupetc. ), a preparation method and use thereof.

Para-phenylalkoxy phenylurea and thiourea compounds and herbicidal use thereof

There are provided certain p-phenylalkoxy phenylurea and thiourea compounds useful for the control of undesirable plants in the presence of agronomic crops and to methods for the preparation of said phenylalkoxy phenylurea and thiourea compounds.