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C9H6ClN3O

Base Information Edit
C<sub>9</sub>H<sub>6</sub>ClN<sub>3</sub>O

Synonyms:C9H6ClN3O

Suppliers and Price of C9H6ClN3O
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of C9H6ClN3O Edit
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Technology Process of C9H6ClN3O

There total 1 articles about C9H6ClN3O 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 5 steps
1.1: methanol / 48 h / 80 °C
2.1: tetrahydrofuran / 1 h / -45 - 0 °C
2.2: 0.5 h / -25 °C
3.1: 1 h / 130 °C
4.1: potassium carbonate / N,N-dimethyl-formamide / 5 h / 100 °C
5.1: hydrogenchloride / 4 h / 80 °C
With hydrogenchloride; potassium carbonate; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2011.01.017
Guidance literature:
Multi-step reaction with 2 steps
1: lithium tert-butoxide / acetone / 24 h / 80 °C
2: N-ethyl-N,N-diisopropylamine / 0 - 150 °C
With N-ethyl-N,N-diisopropylamine; lithium tert-butoxide; In acetone;
DOI:10.1016/j.bmcl.2011.01.017
Guidance literature:
Multi-step reaction with 2 steps
1: lithium tert-butoxide / acetone / 24 h / 80 °C
2: N-ethyl-N,N-diisopropylamine / 0 - 150 °C
With N-ethyl-N,N-diisopropylamine; lithium tert-butoxide; In acetone;
DOI:10.1016/j.bmcl.2011.01.017
upstream raw materials:

2,6-dichloropyridine-4-carboxylic acid

Downstream raw materials:

C20H22N4O2

C20H22N4O2

C21H22N4O

C22H24N4O2

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