- Product Details
Keywords
- Chloroacetamido-2,6-xylidine
- 2,6-Acetoxylidide, 2-chloro- (8CI)
- 2-Chloro-2,6-acetoxylidide
Quick Details
- ProName: 2-Chloro-N-(2,6-dimethylphenyl)acetami...
- CasNo: 1131-01-7
- Molecular Formula: C10H12ClNO
- Appearance: white solid
- Application: (142387-99-3)ranolazine;1-3-(2-Methoxy...
- DeliveryTime: in stock
- PackAge: according to the customer
- Port: shanghai
- ProductionCapacity: 1 Metric Ton/
- Purity: 99%
- Storage: Sealed in dry,Room Temperature
- Transportation: by sea air and courier
- LimitNum: 1 Gram
- Related Substances: 1
- Residue on Ignition: 1
- Heavy Metal: 1
- Valid Period: 1
- 1: 1
- 1: 1
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.