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Methyl 3-aMino-6-chloro-2-Methylisonicotinate

Base Information
  • Chemical Name:Methyl 3-aMino-6-chloro-2-Methylisonicotinate
  • CAS No.:1073182-63-4
  • Molecular Formula:C8H9ClN2O2
  • Molecular Weight:200.62226
  • Hs Code.:
  • Mol file:1073182-63-4.mol
Methyl 3-aMino-6-chloro-2-Methylisonicotinate

Synonyms:Methyl 3-aMino-6-chloro-2-Methylisonicotinate;3-amino-6-chloro-2-methylisonicotinic acid methyl ester

Suppliers and Price of Methyl 3-aMino-6-chloro-2-Methylisonicotinate
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Crysdot
  • Methyl3-amino-6-chloro-2-methylisonicotinate 95+%
  • 1g
  • $ 853.00
  • Chemenu
  • methyl3-amino-6-chloro-2-methylisonicotinate 95%
  • 1g
  • $ 805.00
  • Alichem
  • Methyl3-amino-6-chloro-2-methylisonicotinate
  • 1g
  • $ 2770.00
Total 3 raw suppliers
Chemical Property of Methyl 3-aMino-6-chloro-2-Methylisonicotinate
Chemical Property:
  • PSA:65.21000 
  • LogP:1.99340 
Purity/Quality:

95+% *data from raw suppliers

Methyl3-amino-6-chloro-2-methylisonicotinate 95+% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of Methyl 3-aMino-6-chloro-2-Methylisonicotinate

There total 6 articles about Methyl 3-aMino-6-chloro-2-Methylisonicotinate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With potassium carbonate; tetrakis(triphenylphosphine) palladium(0); In 1,4-dioxane; water; for 7h; Heating / reflux;
Guidance literature:
Multi-step reaction with 6 steps
1.1: tert-butyl alcohol / 12 h / 50 °C
2.1: n-butyllithium; N,N,N,N,-tetramethylethylenediamine / diethyl ether; hexane / -78 - -10 °C
2.2: 0.5 h
2.3: pH ~ 3
3.1: potassium hydroxide; water / 5 h / 90 °C
3.2: 20 °C
4.1: methanol; diethyl ether; toluene / 2 h / 20 °C
5.1: N-Bromosuccinimide / N,N-dimethyl-formamide / 27 h / 20 - 80 °C
6.1: potassium carbonate / tetrakis(triphenylphosphine) palladium(0) / 1,4-dioxane; water / 7 h / Heating / reflux
With potassium hydroxide; N-Bromosuccinimide; n-butyllithium; N,N,N,N,-tetramethylethylenediamine; water; potassium carbonate; tetrakis(triphenylphosphine) palladium(0); In 1,4-dioxane; methanol; diethyl ether; hexane; water; N,N-dimethyl-formamide; toluene; tert-butyl alcohol;
Guidance literature:
Multi-step reaction with 2 steps
1: N-Bromosuccinimide / N,N-dimethyl-formamide / 27 h / 20 - 80 °C
2: potassium carbonate / tetrakis(triphenylphosphine) palladium(0) / 1,4-dioxane; water / 7 h / Heating / reflux
With N-Bromosuccinimide; potassium carbonate; tetrakis(triphenylphosphine) palladium(0); In 1,4-dioxane; water; N,N-dimethyl-formamide;
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