C₁₂H₇BrClFN₄O

Base Information

Chemical Name:C₁₂H₇BrClFN₄O
CAS No.:1372858-48-4
Molecular Formula:C₁₂H₇BrClFN₄O
Molecular Weight:357.569
Hs Code.:

C<sub>12</sub>H<sub>7</sub>BrClFN<sub>4</sub>O

Synonyms:C₁₂H₇BrClFN₄O

Suppliers and Price of C₁₂H₇BrClFN₄O

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₁₂H₇BrClFN₄O

Chemical Property:

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Technology Process of C₁₂H₇BrClFN₄O

There total 5 articles about C₁₂H₇BrClFN₄O 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:

Reference yield:

: 1372858-41-7
C₁₂H₈Br₂ClFN₄O

: 1372858-48-4
C₁₂H₇BrClFN₄O

Guidance literature:: With triethylamine; In tetrahydrofuran; at 20 ℃; for 1h;
DOI:10.1016/j.bmcl.2011.11.067

Reference yield:

: 10071-38-2
6-Chloro-2-methyl-2H-pyridazin-3-one

: 1372858-48-4
C₁₂H₇BrClFN₄O

Guidance literature:: Multi-step reaction with 5 steps

1: hydrazine hydrate / 2 h / 70 °C

2: ethanol / 1 h / Reflux

3: chloroamine-T / tetrahydrofuran; water / 4 h / 65 °C

4: bromine / acetic acid / 2 h / 80 °C

5: triethylamine / tetrahydrofuran / 1 h / 20 °C

With bromine; chloroamine-T; hydrazine hydrate; triethylamine; In tetrahydrofuran; ethanol; water; acetic acid;
DOI:10.1016/j.bmcl.2011.11.067

Reference yield:

: 1245898-36-5
C₅H₈N₄O

: 1372858-48-4
C₁₂H₇BrClFN₄O

Guidance literature:: Multi-step reaction with 4 steps

1: ethanol / 1 h / Reflux

2: chloroamine-T / tetrahydrofuran; water / 4 h / 65 °C

3: bromine / acetic acid / 2 h / 80 °C

4: triethylamine / tetrahydrofuran / 1 h / 20 °C

With bromine; chloroamine-T; triethylamine; In tetrahydrofuran; ethanol; water; acetic acid;
DOI:10.1016/j.bmcl.2011.11.067