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4-[(3-{2-[3-cyano-4-(2-methylpropyl)phenyl]-5-pyrimidinyl}-2-ethylphenyl)oxy]butanoic acid

Base Information
  • Chemical Name:4-[(3-{2-[3-cyano-4-(2-methylpropyl)phenyl]-5-pyrimidinyl}-2-ethylphenyl)oxy]butanoic acid
  • CAS No.:1334607-77-0
  • Molecular Formula:C27H29N3O3
  • Molecular Weight:443.546
  • Hs Code.:
4-[(3-{2-[3-cyano-4-(2-methylpropyl)phenyl]-5-pyrimidinyl}-2-ethylphenyl)oxy]butanoic acid

Synonyms:4-[(3-{2-[3-cyano-4-(2-methylpropyl)phenyl]-5-pyrimidinyl}-2-ethylphenyl)oxy]butanoic acid

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Chemical Property of 4-[(3-{2-[3-cyano-4-(2-methylpropyl)phenyl]-5-pyrimidinyl}-2-ethylphenyl)oxy]butanoic acid
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Technology Process of 4-[(3-{2-[3-cyano-4-(2-methylpropyl)phenyl]-5-pyrimidinyl}-2-ethylphenyl)oxy]butanoic acid

There total 8 articles about 4-[(3-{2-[3-cyano-4-(2-methylpropyl)phenyl]-5-pyrimidinyl}-2-ethylphenyl)oxy]butanoic acid 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:
ethyl 4-[(3-{2-[3-cyano-4-(2-methylpropyl)phenyl]-5-pyrimidinyl}-2-ethylphenyl)oxy]butanoate; With water; lithium hydroxide; In isopropyl alcohol; at 20 ℃; for 2h;
With acetic acid; In isopropyl alcohol;
Guidance literature:
Multi-step reaction with 7 steps
1.1: caesium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / toluene; water / 16 h / 100 °C / Inert atmosphere
2.1: zinc; water; ammonium formate / methanol / 4 h / 80 °C
3.1: sodium nitrite; hydrogen bromide / acetonitrile / 0.5 h / 0 °C
3.2: 16 h / 20 °C
4.1: potassium acetate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / 1,4-dioxane / 12 h / 80 °C / Inert atmosphere
5.1: sodium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,2-dimethoxyethane; water / 90 °C / Inert atmosphere
6.1: potassium phosphate / tetrakis(triphenylphosphine) palladium(0) / 1,2-dimethoxyethane; water / 15 h / 120 °C / Biotage Initiator
7.1: water; lithium hydroxide / isopropyl alcohol / 2 h / 20 °C
With potassium phosphate; water; hydrogen bromide; ammonium formate; potassium acetate; sodium carbonate; caesium carbonate; lithium hydroxide; zinc; sodium nitrite; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; tetrakis(triphenylphosphine) palladium(0); dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; In 1,4-dioxane; methanol; 1,2-dimethoxyethane; water; isopropyl alcohol; toluene; acetonitrile;
Guidance literature:
Multi-step reaction with 5 steps
1.1: sodium nitrite; hydrogen bromide / acetonitrile / 0.5 h / 0 °C
1.2: 16 h / 20 °C
2.1: potassium acetate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / 1,4-dioxane / 12 h / 80 °C / Inert atmosphere
3.1: sodium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,2-dimethoxyethane; water / 90 °C / Inert atmosphere
4.1: potassium phosphate / tetrakis(triphenylphosphine) palladium(0) / 1,2-dimethoxyethane; water / 15 h / 120 °C / Biotage Initiator
5.1: water; lithium hydroxide / isopropyl alcohol / 2 h / 20 °C
With potassium phosphate; water; hydrogen bromide; potassium acetate; sodium carbonate; lithium hydroxide; sodium nitrite; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; tetrakis(triphenylphosphine) palladium(0); dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; In 1,4-dioxane; 1,2-dimethoxyethane; water; isopropyl alcohol; acetonitrile;
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