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Methanone, [1-(1,1-dimethylethyl)-5-hydroxy-1H-pyrazol-4-yl][4'-methoxy-2-methyl-6- (methylsulfonyl)[1,1'-biphenyl]-3-yl]-

Base Information Edit
  • Chemical Name:Methanone, [1-(1,1-dimethylethyl)-5-hydroxy-1H-pyrazol-4-yl][4'-methoxy-2-methyl-6- (methylsulfonyl)[1,1'-biphenyl]-3-yl]-
  • CAS No.:216486-06-5
  • Molecular Formula:C23H26N2O5S
  • Molecular Weight:442.536
  • Hs Code.:
  • Mol file:216486-06-5.mol
Methanone,
[1-(1,1-dimethylethyl)-5-hydroxy-1H-pyrazol-4-yl][4'-methoxy-2-methyl-6-
(methylsulfonyl)[1,1'-biphenyl]-3-yl]-

Synonyms:

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Methanone, [1-(1,1-dimethylethyl)-5-hydroxy-1H-pyrazol-4-yl][4'-methoxy-2-methyl-6- (methylsulfonyl)[1,1'-biphenyl]-3-yl]- Edit
Chemical Property:
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MSDS Files:

SDS file from LookChem

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Technology Process of Methanone, [1-(1,1-dimethylethyl)-5-hydroxy-1H-pyrazol-4-yl][4'-methoxy-2-methyl-6- (methylsulfonyl)[1,1'-biphenyl]-3-yl]-

There total 8 articles about Methanone, [1-(1,1-dimethylethyl)-5-hydroxy-1H-pyrazol-4-yl][4'-methoxy-2-methyl-6- (methylsulfonyl)[1,1'-biphenyl]-3-yl]- 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:
1-(1,1-dimethyl-1-ethyl)-5-hydroxy-1H-pyrazole; 6-methanesulfonyl-4'-methoxy-2-methyl-biphenyl-3-carbonyl chloride; With triethylamine; In dichloromethane; at 5 - 20 ℃;
With potassium carbonate; 2-hydroxy-2-methylpropanenitrile; In acetonitrile;
DOI:10.1002/ps.588
Guidance literature:
Multi-step reaction with 6 steps
1.1: 86 percent / Pd(OAc)2; NaHCO3; 1,4-bis(diphenylphosphino)butane / 2-methyl-propan-2-ol; H2O / 20 h / 125 °C / 15001.2 Torr
2.1: 68 percent / NH4OH; CuO / H2O / 17 h / 180 °C
3.1: NaNO2; H2SO4 / H2O / 30 h / 5 °C
3.2: 90 percent / KI / H2O / 0.5 h / 80 °C
4.1: 84 percent / K2CO3 / Pd(OAc)2; P(o-Tol)3 / bis-(2-methoxy-ethyl) ether; H2O / 12 h / 95 °C
5.1: SOCl2 / 1,2-dichloro-ethane / 3 h / Heating
6.1: (CH3CH2)3N / CH2Cl2 / 5 - 20 °C
6.2: 10.9 g / K2CO3 / (CH3)2C(CN)OH / acetonitrile
With palladium diacetate; ammonium hydroxide; thionyl chloride; sulfuric acid; sodium hydrogencarbonate; potassium carbonate; triethylamine; 1,4-di(diphenylphosphino)-butane; copper(II) oxide; sodium nitrite; palladium diacetate; tris-(o-tolyl)phosphine; In dichloromethane; diethylene glycol dimethyl ether; water; 1,2-dichloro-ethane; tert-butyl alcohol; 4.1: Suzuki condensation;
DOI:10.1002/ps.588
Guidance literature:
Multi-step reaction with 4 steps
1.1: NaNO2; H2SO4 / H2O / 30 h / 5 °C
1.2: 90 percent / KI / H2O / 0.5 h / 80 °C
2.1: 84 percent / K2CO3 / Pd(OAc)2; P(o-Tol)3 / bis-(2-methoxy-ethyl) ether; H2O / 12 h / 95 °C
3.1: SOCl2 / 1,2-dichloro-ethane / 3 h / Heating
4.1: (CH3CH2)3N / CH2Cl2 / 5 - 20 °C
4.2: 10.9 g / K2CO3 / (CH3)2C(CN)OH / acetonitrile
With thionyl chloride; sulfuric acid; potassium carbonate; triethylamine; sodium nitrite; palladium diacetate; tris-(o-tolyl)phosphine; In dichloromethane; diethylene glycol dimethyl ether; water; 1,2-dichloro-ethane; 2.1: Suzuki condensation;
DOI:10.1002/ps.588
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