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(E)-3-{4-[1-(4-tert-butylcyclohexyl)-3-methyl-5-oxo-4,5-dihydro-1H-pyrazol-4-ylazo]-3-hydroxyphenyl}-2-methylacrylic acid

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  • Chemical Name:(E)-3-{4-[1-(4-tert-butylcyclohexyl)-3-methyl-5-oxo-4,5-dihydro-1H-pyrazol-4-ylazo]-3-hydroxyphenyl}-2-methylacrylic acid
  • CAS No.:634902-48-0
  • Molecular Formula:C24H32N4O4
  • Molecular Weight:440.542
  • Hs Code.:
(E)-3-{4-[1-(4-tert-butylcyclohexyl)-3-methyl-5-oxo-4,5-dihydro-1H-pyrazol-4-ylazo]-3-hydroxyphenyl}-2-methylacrylic acid

Synonyms:(E)-3-{4-[1-(4-tert-butylcyclohexyl)-3-methyl-5-oxo-4,5-dihydro-1H-pyrazol-4-ylazo]-3-hydroxyphenyl}-2-methylacrylic acid

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Chemical Property of (E)-3-{4-[1-(4-tert-butylcyclohexyl)-3-methyl-5-oxo-4,5-dihydro-1H-pyrazol-4-ylazo]-3-hydroxyphenyl}-2-methylacrylic acid
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Technology Process of (E)-3-{4-[1-(4-tert-butylcyclohexyl)-3-methyl-5-oxo-4,5-dihydro-1H-pyrazol-4-ylazo]-3-hydroxyphenyl}-2-methylacrylic acid

There total 5 articles about (E)-3-{4-[1-(4-tert-butylcyclohexyl)-3-methyl-5-oxo-4,5-dihydro-1H-pyrazol-4-ylazo]-3-hydroxyphenyl}-2-methylacrylic 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:
C10H11NO3*ClH; With hydrogenchloride; sodium nitrite; In ethanol; water; at 0 ℃; for 0.25h;
2-(4-tert-butyl-cyclohexyl)-5-methyl-2,4-dihydro-pyrazol-3-one; In ethanol; water; at 20 ℃; for 18h; pH=8; Alkaline conditions;
Guidance literature:
Multi-step reaction with 5 steps
1.1: dichloromethane / 18 h / Presence of drying agents
2.1: hydrogen / palladium 10% on activated carbon / tetrahydrofuran / 18 h / 2585.81 Torr
3.1: trifluoroacetic acid / dichloromethane / 5 h / 20 °C
4.1: acetic acid / 18 h / 100 °C
5.1: hydrogenchloride; sodium nitrite / ethanol; water / 0.25 h / 0 °C
5.2: 18 h / 20 °C / pH 8 / Alkaline conditions
With hydrogenchloride; hydrogen; trifluoroacetic acid; sodium nitrite; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; dichloromethane; water; acetic acid;
Guidance literature:
Multi-step reaction with 4 steps
1.1: hydrogen / palladium 10% on activated carbon / tetrahydrofuran / 18 h / 2585.81 Torr
2.1: trifluoroacetic acid / dichloromethane / 5 h / 20 °C
3.1: acetic acid / 18 h / 100 °C
4.1: hydrogenchloride; sodium nitrite / ethanol; water / 0.25 h / 0 °C
4.2: 18 h / 20 °C / pH 8 / Alkaline conditions
With hydrogenchloride; hydrogen; trifluoroacetic acid; sodium nitrite; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; dichloromethane; water; acetic acid;
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