6-(4-Bromo-phenyl)-4-cyclopropyl-2-imino-cyclohex-3-ene-1,1,3-tricarbonitrile

Base Information

Chemical Name:6-(4-Bromo-phenyl)-4-cyclopropyl-2-imino-cyclohex-3-ene-1,1,3-tricarbonitrile
CAS No.:136494-56-9
Molecular Formula:C₁₈H₁₃BrN₄
Molecular Weight:365.232
Hs Code.:

Synonyms:6-(4-Bromo-phenyl)-4-cyclopropyl-2-imino-cyclohex-3-ene-1,1,3-tricarbonitrile

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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 6-(4-Bromo-phenyl)-4-cyclopropyl-2-imino-cyclohex-3-ene-1,1,3-tricarbonitrile

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Technology Process of 6-(4-Bromo-phenyl)-4-cyclopropyl-2-imino-cyclohex-3-ene-1,1,3-tricarbonitrile

There total 1 articles about 6-(4-Bromo-phenyl)-4-cyclopropyl-2-imino-cyclohex-3-ene-1,1,3-tricarbonitrile 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: 77.0%

: 17407-30-6
2-(1-cyclopropylethylidene)malononitrile

: 2826-24-6
4-bromobenzylidenemalononitrile

: 136494-56-9
6-(4-Bromo-phenyl)-4-cyclopropyl-2-imino-cyclohex-3-ene-1,1,3-tricarbonitrile

Guidance literature:: With morpholine; In methanol; at 25 ℃; for 1h;

Reference yield: 47.0%

: 136494-56-9
6-(4-Bromo-phenyl)-4-cyclopropyl-2-imino-cyclohex-3-ene-1,1,3-tricarbonitrile

: 136494-65-0
(2E,4E)-2-(1-Amino-2,2-dicyano-vinyl)-5-(4-bromo-phenyl)-3-cyclopropyl-penta-2,4-dienenitrile

Guidance literature:: With o-xylene; for 0.5h; Heating;

Reference yield:

: 136494-56-9
6-(4-Bromo-phenyl)-4-cyclopropyl-2-imino-cyclohex-3-ene-1,1,3-tricarbonitrile

: 136494-70-7
2-[6-(4-Bromo-phenyl)-3-cyano-4-cyclopropyl-1H-pyridin-2-ylidene]-malononitrile

Guidance literature:: Multi-step reaction with 2 steps

1: 47 percent / o-xylene / 0.5 h / Heating

2: 42 percent / triethylamine / o-xylene / 0.5 h / Heating

With o-xylene; triethylamine; In o-xylene;