cyclohexyl 1-(4-hydroxy-4-(1-(4-methoxyphenyl)-5-(p-tolyl)-1H-pyrazol-3-yl)-cis-cyclohexyloxy)ethyl carbonate

Base Information

Chemical Name:cyclohexyl 1-(4-hydroxy-4-(1-(4-methoxyphenyl)-5-(p-tolyl)-1H-pyrazol-3-yl)-cis-cyclohexyloxy)ethyl carbonate
CAS No.:1224949-16-9
Molecular Formula:C₃₂H₄₀N₂O₆
Molecular Weight:548.679
Hs Code.:

Synonyms:cyclohexyl 1-(4-hydroxy-4-(1-(4-methoxyphenyl)-5-(p-tolyl)-1H-pyrazol-3-yl)-cis-cyclohexyloxy)ethyl carbonate

Suppliers and Price of cyclohexyl 1-(4-hydroxy-4-(1-(4-methoxyphenyl)-5-(p-tolyl)-1H-pyrazol-3-yl)-cis-cyclohexyloxy)ethyl carbonate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of cyclohexyl 1-(4-hydroxy-4-(1-(4-methoxyphenyl)-5-(p-tolyl)-1H-pyrazol-3-yl)-cis-cyclohexyloxy)ethyl carbonate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of cyclohexyl 1-(4-hydroxy-4-(1-(4-methoxyphenyl)-5-(p-tolyl)-1H-pyrazol-3-yl)-cis-cyclohexyloxy)ethyl carbonate

There total 8 articles about cyclohexyl 1-(4-hydroxy-4-(1-(4-methoxyphenyl)-5-(p-tolyl)-1H-pyrazol-3-yl)-cis-cyclohexyloxy)ethyl carbonate 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: 5.1%

: 1224948-06-4
1-(1-(4-methoxyphenyl)-5-(p-tolyl)-1H-pyrazol-3-yl)cyclohexane-cis-1,4-diol

: 95789-69-8,102672-57-1
cyclohexyl (1-iodoethyl)carbonate

: 1224949-16-9
cyclohexyl 1-(4-hydroxy-4-(1-(4-methoxyphenyl)-5-(p-tolyl)-1H-pyrazol-3-yl)-cis-cyclohexyloxy)ethyl carbonate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; silver(I) chloride; In 1,2-dichloro-ethane; at 80 ℃; for 12h;

Reference yield:

: 1224949-51-2
8-(1-(4-methoxyphenyl)-5-(p-tolyl)-1H-pyrazol-3-yl)-1,4-dioxaspiro[4.5]decan-8-ol

: 1224949-16-9
cyclohexyl 1-(4-hydroxy-4-(1-(4-methoxyphenyl)-5-(p-tolyl)-1H-pyrazol-3-yl)-cis-cyclohexyloxy)ethyl carbonate

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogenchloride; water / tetrahydrofuran / 15 h / 20 °C

1.2: 0 °C

2.1: sodium tetrahydroborate; methanol / 2 h / 20 °C

3.1: N-ethyl-N,N-diisopropylamine; silver(I) chloride / 1,2-dichloro-ethane / 12 h / 80 °C

With hydrogenchloride; methanol; sodium tetrahydroborate; water; N-ethyl-N,N-diisopropylamine; silver(I) chloride; In tetrahydrofuran; 1,2-dichloro-ethane;

Reference yield:

: 1224949-36-3
3-(8-hydroxy-1,4-dioxaspiro[4.5]decan-8-yl)-1-(p-tolyl)-2-propyn-1-one

: 1224949-16-9
cyclohexyl 1-(4-hydroxy-4-(1-(4-methoxyphenyl)-5-(p-tolyl)-1H-pyrazol-3-yl)-cis-cyclohexyloxy)ethyl carbonate

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine / ethanol / 0.5 h / 20 °C

1.2: 15 h / 20 °C

2.1: hydrogenchloride; water / tetrahydrofuran / 15 h / 20 °C

2.2: 0 °C

3.1: sodium tetrahydroborate; methanol / 2 h / 20 °C

4.1: N-ethyl-N,N-diisopropylamine; silver(I) chloride / 1,2-dichloro-ethane / 12 h / 80 °C

With hydrogenchloride; methanol; sodium tetrahydroborate; water; triethylamine; N-ethyl-N,N-diisopropylamine; silver(I) chloride; In tetrahydrofuran; ethanol; 1,2-dichloro-ethane;