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O,O-dimethyl 3-bromo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carbonylcarbamoylphosphoramidothioate

Base Information Edit
  • Chemical Name:O,O-dimethyl 3-bromo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carbonylcarbamoylphosphoramidothioate
  • CAS No.:1438853-60-1
  • Molecular Formula:C12H12BrClN5O4PS
  • Molecular Weight:468.655
  • Hs Code.:
  • Mol file:1438853-60-1.mol
O,O-dimethyl 3-bromo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carbonylcarbamoylphosphoramidothioate

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Chemical Property of O,O-dimethyl 3-bromo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carbonylcarbamoylphosphoramidothioate Edit
Chemical Property:
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Technology Process of O,O-dimethyl 3-bromo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carbonylcarbamoylphosphoramidothioate

There total 8 articles about O,O-dimethyl 3-bromo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carbonylcarbamoylphosphoramidothioate 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:
Multi-step reaction with 8 steps
1: sodium ethanolate / ethanol / Reflux
2: trichlorophosphate / acetonitrile / 80 °C
3: dipotassium peroxodisulfate; sulfuric acid / acetonitrile / Reflux
4: sodium hydroxide / water; methanol
5: N,N-dimethyl-formamide; oxalyl dichloride / dichloromethane / 3 h / 20 °C
6: ammonium hydroxide / water; tetrahydrofuran / 0 °C
7: 1,2-dichloro-ethane / 2 h / Reflux
8: monoethylene glycol diethyl ether / Reflux
With ammonium hydroxide; dipotassium peroxodisulfate; oxalyl dichloride; sulfuric acid; sodium ethanolate; N,N-dimethyl-formamide; sodium hydroxide; trichlorophosphate; In tetrahydrofuran; methanol; ethanol; dichloromethane; monoethylene glycol diethyl ether; water; 1,2-dichloro-ethane; acetonitrile;
DOI:10.1021/jf4012467
Guidance literature:
Multi-step reaction with 7 steps
1: trichlorophosphate / acetonitrile / 80 °C
2: dipotassium peroxodisulfate; sulfuric acid / acetonitrile / Reflux
3: sodium hydroxide / water; methanol
4: N,N-dimethyl-formamide; oxalyl dichloride / dichloromethane / 3 h / 20 °C
5: ammonium hydroxide / water; tetrahydrofuran / 0 °C
6: 1,2-dichloro-ethane / 2 h / Reflux
7: monoethylene glycol diethyl ether / Reflux
With ammonium hydroxide; dipotassium peroxodisulfate; oxalyl dichloride; sulfuric acid; N,N-dimethyl-formamide; sodium hydroxide; trichlorophosphate; In tetrahydrofuran; methanol; dichloromethane; monoethylene glycol diethyl ether; water; 1,2-dichloro-ethane; acetonitrile;
DOI:10.1021/jf4012467
Guidance literature:
Multi-step reaction with 6 steps
1: dipotassium peroxodisulfate; sulfuric acid / acetonitrile / Reflux
2: sodium hydroxide / water; methanol
3: N,N-dimethyl-formamide; oxalyl dichloride / dichloromethane / 3 h / 20 °C
4: ammonium hydroxide / water; tetrahydrofuran / 0 °C
5: 1,2-dichloro-ethane / 2 h / Reflux
6: monoethylene glycol diethyl ether / Reflux
With ammonium hydroxide; dipotassium peroxodisulfate; oxalyl dichloride; sulfuric acid; N,N-dimethyl-formamide; sodium hydroxide; In tetrahydrofuran; methanol; dichloromethane; monoethylene glycol diethyl ether; water; 1,2-dichloro-ethane; acetonitrile;
DOI:10.1021/jf4012467
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