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3-(4-(7H-pyrrolo[2,3-c]pyridazin-4-yl)-1H-pyrazol-1-yl)-4-cyclohexylbutane nitrile

Base Information
  • Chemical Name:3-(4-(7H-pyrrolo[2,3-c]pyridazin-4-yl)-1H-pyrazol-1-yl)-4-cyclohexylbutane nitrile
  • CAS No.:1269823-37-1
  • Molecular Formula:C19H22N6
  • Molecular Weight:334.424
  • Hs Code.:
3-(4-(7H-pyrrolo[2,3-c]pyridazin-4-yl)-1H-pyrazol-1-yl)-4-cyclohexylbutane nitrile

Synonyms:3-(4-(7H-pyrrolo[2,3-c]pyridazin-4-yl)-1H-pyrazol-1-yl)-4-cyclohexylbutane nitrile

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Chemical Property of 3-(4-(7H-pyrrolo[2,3-c]pyridazin-4-yl)-1H-pyrazol-1-yl)-4-cyclohexylbutane nitrile
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Technology Process of 3-(4-(7H-pyrrolo[2,3-c]pyridazin-4-yl)-1H-pyrazol-1-yl)-4-cyclohexylbutane nitrile

There total 14 articles about 3-(4-(7H-pyrrolo[2,3-c]pyridazin-4-yl)-1H-pyrazol-1-yl)-4-cyclohexylbutane nitrile 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 11 steps
1.1: methanol / 0.5 h / 20 °C
1.2: 20 °C
2.1: acetic acid; iron / 0.5 h / 45 - 100 °C
3.1: sodium nitrite / water; acetic acid / 48 h / 18 - 65 °C
4.1: potassium hydroxide / 0.5 h / 70 °C
4.2: 20 °C
5.1: trifluoroacetic acid / 48 h / 230 °C / Sealed ampoule
6.1: trichlorophosphate; N-benzyl-N,N,N-triethylammonium chloride; N,N-dimethyl-aniline / acetonitrile / 2 h / 80 °C
7.1: dmap; triethylamine / dichloromethane / -10 - 50 °C
8.1: potassium carbonate; water / tetrakis(triphenylphosphine) palladium(0) / 1,4-dioxane / 2 h / 80 °C / Inert atmosphere
9.1: hydrogenchloride / water; tetrahydrofuran / 10 h / 20 °C
10.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / 20 °C
11.1: sodium hydroxide / methanol / 3 h / 20 °C
With hydrogenchloride; dmap; N-benzyl-N,N,N-triethylammonium chloride; water; iron; potassium carbonate; acetic acid; N,N-dimethyl-aniline; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; trifluoroacetic acid; potassium hydroxide; sodium hydroxide; sodium nitrite; trichlorophosphate; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; water; acetic acid; acetonitrile;
Guidance literature:
Multi-step reaction with 10 steps
1.1: acetic acid; iron / 0.5 h / 45 - 100 °C
2.1: sodium nitrite / water; acetic acid / 48 h / 18 - 65 °C
3.1: potassium hydroxide / 0.5 h / 70 °C
3.2: 20 °C
4.1: trifluoroacetic acid / 48 h / 230 °C / Sealed ampoule
5.1: trichlorophosphate; N-benzyl-N,N,N-triethylammonium chloride; N,N-dimethyl-aniline / acetonitrile / 2 h / 80 °C
6.1: dmap; triethylamine / dichloromethane / -10 - 50 °C
7.1: potassium carbonate; water / tetrakis(triphenylphosphine) palladium(0) / 1,4-dioxane / 2 h / 80 °C / Inert atmosphere
8.1: hydrogenchloride / water; tetrahydrofuran / 10 h / 20 °C
9.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / 20 °C
10.1: sodium hydroxide / methanol / 3 h / 20 °C
With hydrogenchloride; dmap; N-benzyl-N,N,N-triethylammonium chloride; water; iron; potassium carbonate; acetic acid; N,N-dimethyl-aniline; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; trifluoroacetic acid; potassium hydroxide; sodium hydroxide; sodium nitrite; trichlorophosphate; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; water; acetic acid; acetonitrile;
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