CasNo.1131-01-7,2-Chloro-N-(2,6-dimethylphenyl)acetamide,(1131-01-7) Suppliers

1 Gram	Negotiable

Min.Order :1 Gram
Purity: 99%
Payment Terms : T/T

Keywords

Chloroacetamido-2,6-xylidine 2,6-Acetoxylidide, 2-chloro- (8CI) 2-Chloro-2,6-acetoxylidide

Quick Details

Appearance:white solid
Application:(142387-99-3)ranolazine;1-3-(2-Methoxyphenoxy)-2-hydroxypropyl-4-...;1-Piperazineacetamide,N-(2,6-dimethylphenyl)-4-[2-hydroxy-3-(2-methoxyphenoxy)propyl]-;N-(2,6-dimethylphenyl)-2-[4-[2-hydroxy-3-(2-
PackAge:according to the customer
ProductionCapacity:1|Metric Ton|
Storage:Sealed in dry,Room Temperature
Transportation:by sea air and courier

Superiority:

useusedaspharmaceuticalintermediates.ProductionmethodItisobtainedbythereactionof2,6-dimethylanilineandchloroacetylchloride:anhydrousbenzeneand2,6-dimethylanilinearecooledtobelow28°C,chloroacetylchlorideissChemicalbooklowlydroppedunderstirring,thetemperaturedoesnotexceed30°C,theadditioniscompleted,thestirringreactionis1h,andthenheatedandrefluxedfor8h.Coolingcrystallization,filtration,anddryingtoobtainthefinishedproduct.useusedaspharmaceuticalintermediates.ProductionmethodItisobtainedbythereactionof2,6-dimethylanilineandchloroacetylchloride:anhydrousbenzeneand2,6-dimethylanilinearecooledtobelow28°C,chloroacetylchlorideissChemicalbooklowlydroppedunderstirring,thetemperaturedoesnotexceed30°C,theadditioniscompleted,thestirringreactionis1h,andthenheatedandrefluxedfor8h.Coolingcrystallization,filtration,anddryingtoobtainthefinishedproduct.useusedaspharmaceuticalintermediates.ProductionmethodItisobtainedbythereactionof2,6-dimethylanilineandchloroacetylchloride:anhydrousbenzeneand2,6-dimethylanilinearecooledtobelow28°C,chloroacetylchlorideissChemicalbooklowlydroppedunderstirring,thetemperaturedoesnotexceed30°C,theadditioniscompleted,thestirringreactionis1h,andthenheatedandrefluxedfor8h.Coolingcrystallization,filtration,anddryingtoobtainthefinishedproduct.useusedaspharmaceuticalintermediates.ProductionmethodItisobtainedbythereactionof2,6-dimethylanilineandchloroacetylchloride:anhydrousbenzeneand2,6-dimethylanilinearecooledtobelow28°C,chloroacetylchlorideissChemicalbooklowlydroppedunderstirring,thetemperaturedoesnotexceed30°C,theadditioniscompleted,thestirringreactionis1h,andthenheatedandrefluxedfor8h.Coolingcrystallization,filtration,anddryingtoobtainthefinishedproduct.

Details:

useusedaspharmaceuticalintermediates.ProductionmethodItisobtainedbythereactionof2,6-dimethylanilineandchloroacetylchloride:anhydrousbenzeneand2,6-dimethylanilinearecooledtobelow28°C,chloroacetylchlorideissChemicalbooklowlydroppedunderstirring,thetemperaturedoesnotexceed30°C,theadditioniscompleted,thestirringreactionis1h,andthenheatedandrefluxedfor8h.Coolingcrystallization,filtration,anddryingtoobtainthefinishedproduct.useusedaspharmaceuticalintermediates.ProductionmethodItisobtainedbythereactionof2,6-dimethylanilineandchloroacetylchloride:anhydrousbenzeneand2,6-dimethylanilinearecooledtobelow28°C,chloroacetylchlorideissChemicalbooklowlydroppedunderstirring,thetemperaturedoesnotexceed30°C,theadditioniscompleted,thestirringreactionis1h,andthenheatedandrefluxedfor8h.Coolingcrystallization,filtration,anddryingtoobtainthefinishedproduct.useusedaspharmaceuticalintermediates.ProductionmethodItisobtainedbythereactionof2,6-dimethylanilineandchloroacetylchloride:anhydrousbenzeneand2,6-dimethylanilinearecooledtobelow28°C,chloroacetylchlorideissChemicalbooklowlydroppedunderstirring,thetemperaturedoesnotexceed30°C,theadditioniscompleted,thestirringreactionis1h,andthenheatedandrefluxedfor8h.Coolingcrystallization,filtration,anddryingtoobtainthefinishedproduct.