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N10-nitrosopteroyl azide

Base Information Edit
  • Chemical Name:N10-nitrosopteroyl azide
  • CAS No.:197151-80-7
  • Molecular Formula:C14H10N10O3
  • Molecular Weight:366.299
  • Hs Code.:
  • Mol file:197151-80-7.mol
N<sup>10</sup>-nitrosopteroyl azide

Synonyms:N10-nitrosopteroyl azide

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of N10-nitrosopteroyl azide Edit
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Technology Process of N10-nitrosopteroyl azide

There total 5 articles about N10-nitrosopteroyl azide 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 tert.-butylnitrite; potassium thioacyanate; In trifluoroacetic acid; at -10 ℃; for 4h;
DOI:10.1021/ja971568j
Guidance literature:
Multi-step reaction with 4 steps
1.1: tetrahydrofuran / 10.5 h / 0 - 25 °C
1.2: 123 g / ice / tetrahydrofuran / 3 h / 25 °C
2.1: 89 percent / aq. cesium carbonate / dimethylformamide / 5 h / 25 °C
3.1: 90 percent / hydrazine / dimethylsulfoxide-d6 / 9 h / 25 °C
4.1: potassium thiocyanate; tert-butyl nitrite / trifluoroacetic acid / 4 h / -10 °C
With tert.-butylnitrite; potassium thioacyanate; caesium carbonate; hydrazine; In tetrahydrofuran; dimethylsulfoxide-d6; N,N-dimethyl-formamide; trifluoroacetic acid; 1.1: Acylation / 1.2: Hydrolysis / 2.1: Hydrolysis / 3.1: hydrazinolysis / 4.1: Nitrosation;
DOI:10.1021/ja971568j
Guidance literature:
Multi-step reaction with 5 steps
1.1: 67 percent / tetramethylguanidine / dimethylsulfoxide / 9 h / 25 °C
2.1: tetrahydrofuran / 10.5 h / 0 - 25 °C
2.2: 123 g / ice / tetrahydrofuran / 3 h / 25 °C
3.1: 89 percent / aq. cesium carbonate / dimethylformamide / 5 h / 25 °C
4.1: 90 percent / hydrazine / dimethylsulfoxide-d6 / 9 h / 25 °C
5.1: potassium thiocyanate; tert-butyl nitrite / trifluoroacetic acid / 4 h / -10 °C
With tert.-butylnitrite; 1,1,3,3-tetramethylguanidine; potassium thioacyanate; caesium carbonate; hydrazine; In tetrahydrofuran; dimethylsulfoxide-d6; dimethyl sulfoxide; N,N-dimethyl-formamide; trifluoroacetic acid; 1.1: Acylation / 2.1: Acylation / 2.2: Hydrolysis / 3.1: Hydrolysis / 4.1: hydrazinolysis / 5.1: Nitrosation;
DOI:10.1021/ja971568j
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