49656-34-0

Usage

InChI:InChI=1/C9H6ClNOS/c10-7-3-1-6(2-4-7)8-5-11-9(13)12-8/h1-5H,(H,11,13)

Upstream product

• 104-88-1 4-chlorobenzaldehyde 
• 90985-86-7 phenylthio(trimethylsilyl)methyl isothiocyanate 
• 463-71-8 thiophosgene 
• 5467-71-0 4-chlorophenacylamine hydrochloride 

Downstream Products

• 126767-45-1 2-Bromodifluoromethylthio-5-(4-chlorophenyl)oxazole 
• 126767-47-3 5-(4-Chlorophenyl)-2-(2,2,2-trifluoroethylthio)oxazole 
• 126767-46-2 5-(4-Chlorophenyl)-2-difluoromethylthiooxazole 
• 1240282-86-3 2-chloro-5-(4-chlorophenyl)oxazole 

Relevant academic research and scientific papers

Compositions and Methods for Controlling Nematodes

Compositions and processes for controlling nematodes are described herein, e.g., nematodes that infest plants or animals. The compounds include oxazoles, oxadiazoles and thiadiazoles.

Pyrimidine derivatives exhibiting antitumor activity

A compound represented by the formula (I): wherein, for example, R1, R2, R3, and R4 are each independently hydrogen atom, alky, and the like, R5 and R6 are each independently hydrogen atom, alkyl, and the like, X is —O—, —S—, and the like, Y is 5-membered heteroaryl-diyl and the like, Z is optionally substituted aryl and the like, the prodrugs thereof, or their pharmaceutically acceptable salts, or their solvates.

Chloro(phenylthio)methyltrimethylsilane: Preparation and some Synthetic Reactions

Reaction of the title compound (2) with lead thiocyanate gave phenylthio(trimethylsilyl)methyl isothiocyanate (3) which further reacted with aromatic aldehydes in the presence of fluoride ion to afford oxazoles in good yields.Compound (2) also reacted with silyl enol ethers to give β-silyl ketones which were capable of being converted into β-functionalized vinylsilanes.