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3-AMino-6-chloro-2-Methylisonicotinic acid

Base Information
  • Chemical Name:3-AMino-6-chloro-2-Methylisonicotinic acid
  • CAS No.:1073182-66-7
  • Molecular Formula:C7H7ClN2O2
  • Molecular Weight:186.59568
  • Hs Code.:
  • Mol file:1073182-66-7.mol
3-AMino-6-chloro-2-Methylisonicotinic acid

Synonyms:3-AMino-6-chloro-2-Methylisonicotinic acid

Suppliers and Price of 3-AMino-6-chloro-2-Methylisonicotinic acid
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
  • 3-Amino-6-chloro-2-methylisonicotinicacid 95+%
  • 1g
  • $ 853.00
  • Chemenu
  • 3-amino-6-chloro-2-methylisonicotinicacid 95%
  • 1g
  • $ 805.00
Total 3 raw suppliers
Chemical Property of 3-AMino-6-chloro-2-Methylisonicotinic acid
Chemical Property:
  • PSA:76.21000 
  • LogP:1.90500 
Purity/Quality:

95+% *data from raw suppliers

3-Amino-6-chloro-2-methylisonicotinicacid 95+% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 3-AMino-6-chloro-2-Methylisonicotinic acid

There total 7 articles about 3-AMino-6-chloro-2-Methylisonicotinic acid 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:
3-amino-6-chloro-2-methylisonicotinic acid methyl ester; With methanol; sodium hydroxide; water; for 2.5h; Heating / reflux;
With hydrogenchloride; water; at 20 ℃;
Guidance literature:
Multi-step reaction with 7 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
7.1: methanol; sodium hydroxide; water / 2.5 h / Heating / reflux
7.2: 20 °C
With methanol; potassium hydroxide; sodium 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 3 steps
1.1: N-Bromosuccinimide / N,N-dimethyl-formamide / 27 h / 20 - 80 °C
2.1: potassium carbonate / tetrakis(triphenylphosphine) palladium(0) / 1,4-dioxane; water / 7 h / Heating / reflux
3.1: methanol; sodium hydroxide; water / 2.5 h / Heating / reflux
3.2: 20 °C
With methanol; sodium hydroxide; N-Bromosuccinimide; water; potassium carbonate; tetrakis(triphenylphosphine) palladium(0); In 1,4-dioxane; water; N,N-dimethyl-formamide;
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