887623-58-7

Basic information

• Product Name: 1-Piperazinecarboxamide, 4-[4-(2,4-difluorophenyl)-2-thiazolyl]-N-(3,4-dimethyl-5-isoxazolyl)-
• CAS NO: 887623-58-7
• Molecular Formula: C19H19F2N5O2S
• Molecular Weight: 419.455
• Mol File: 887623-58-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-Piperazinecarboxamide, 4-[4-(2,4-difluorophenyl)-2-thiazolyl]-N-(3,4-dimethyl-5-isoxazolyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Piperazinecarboxamide, 4-[4-(2,4-difluorophenyl)-2-thiazolyl]-N-(3,4-dimethyl-5-isoxazolyl)-(887623-58-7)
• EPA Substance Registry System: 1-Piperazinecarboxamide, 4-[4-(2,4-difluorophenyl)-2-thiazolyl]-N-(3,4-dimethyl-5-isoxazolyl)-(887623-58-7)

Safety Data

• Hazardous Substances Data: 887623-58-7(Hazardous Substances Data)

Upstream product

• 887624-70-6 N-(3,4-dimethylisoxazol-5-yl)piperazine-1-carboxamide 
• 887625-49-2 1-(2,4-difluorophenyl)-2-thiocyanatoethanone 
• 399-53-1 2,4-difluorobenzaldehyde 
• 887625-51-6 tert-butyl 4-[4-(2,4-difluorophenyl)thiazol-2-yl]piperazine-1-carboxylate 
• 19947-75-2 5-amino-3,4-dimethylisoxazol 
• 887625-50-5 2-bromo-4-(2,4-difluorophenyl)thiazole 
• 102429-07-2 2-bromo-2',4'-difluoroacetophenone 
• 887624-58-0 2,2,2-trichloroethyl (3,4-dimethylisoxazol-5-yl)carbamate 
• 887625-52-7 4-(2,4-difluorophenyl)-2-(piperazin-1-yl)thiazole 

Relevant articles and documents

A 2-thiocyano HYPNONE derivatives method for the preparation of

The invention discloses a method for preparing 2-sulfur cyano acetophenone derivatives. The method for preparing the 2-sulfur cyano acetophenone derivatives comprises the following steps: dissolving styrene derivatives and ammonium thiocyanate in a solvent, and reacting at 20-30 DEG C to obtain 2-sulfur cyano acetophenone derivatives. According to the method for preparing the 2-sulfur cyano acetophenone derivatives, the styrene derivatives are taken as starting materials; the raw materials are easily available and various in type; products prepared by the method have various in type, can be directly used and can also be used for other further reactions; meanwhile, the method is mild in reaction conditions and simple in reaction operation and post-processing process; an accelerant does not need to be added; the production process meets the green and chemical requirements, is relatively high in yield and is suitable for large-scale production.