C₂₃H₃₃N₃O₂

Base Information

Chemical Name:C₂₃H₃₃N₃O₂
CAS No.:958841-22-0
Molecular Formula:C₂₃H₃₃N₃O₂
Molecular Weight:383.534
Hs Code.:

C<sub>23</sub>H<sub>33</sub>N<sub>3</sub>O<sub>2</sub>

Synonyms:

Suppliers and Price of C₂₃H₃₃N₃O₂

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

Crysdot
(3-Isopropoxyphenyl)(1-((5-methyl-1-propyl-1H-pyrazol-4-yl)methyl)piperidin-3-yl)methanone 95+%
1g
$ 2957.00

Alichem
(3-Isopropoxyphenyl)(1-((5-methyl-1-propyl-1H-pyrazol-4-yl)methyl)piperidin-3-yl)methanone
1g
$ 3248.20

Total 1 raw suppliers

Chemical Property of C₂₃H₃₃N₃O₂

Chemical Property:

Purity/Quality:

95+% ^*data from raw suppliers

(3-Isopropoxyphenyl)(1-((5-methyl-1-propyl-1H-pyrazol-4-yl)methyl)piperidin-3-yl)methanone 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₃H₃₃N₃O₂

There total 3 articles about C₂₃H₃₃N₃O₂ 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:

: 1350920-21-6
tert-butyl 3-(3-isopropoxybenzoyl)piperidine-1-carboxylate

: 958841-22-0
C₂₃H₃₃N₃O₂

Guidance literature:: Multi-step reaction with 2 steps

1: trifluoroacetic acid / dichloromethane / 10 h

2: sodium cyanoborohydride / 1,2-dichloro-ethane / 2 h / 20 °C / Inert atmosphere

With sodium cyanoborohydride; trifluoroacetic acid; In dichloromethane; 1,2-dichloro-ethane;
DOI:10.1016/j.bmcl.2011.09.057

Reference yield:

: 71381-75-4,88495-54-9,84358-12-3
N-(tert-butyloxycarbonyl)nipecotic acid

: 958841-22-0
C₂₃H₃₃N₃O₂

Guidance literature:: Multi-step reaction with 3 steps

1: tetrahydrofuran / 20 °C / Inert atmosphere; Cooling with acetone-dry ice

2: trifluoroacetic acid / dichloromethane / 10 h

3: sodium cyanoborohydride / 1,2-dichloro-ethane / 2 h / 20 °C / Inert atmosphere

With sodium cyanoborohydride; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; 1,2-dichloro-ethane;
DOI:10.1016/j.bmcl.2011.09.057

Reference yield:

: 498-95-3,262853-93-0
nipecotic acid

: 958841-22-0
C₂₃H₃₃N₃O₂

Guidance literature:: Multi-step reaction with 4 steps

1: sodium hydroxide / 1,4-dioxane; water / 15 h

2: tetrahydrofuran / 20 °C / Inert atmosphere; Cooling with acetone-dry ice

3: trifluoroacetic acid / dichloromethane / 10 h

4: sodium cyanoborohydride / 1,2-dichloro-ethane / 2 h / 20 °C / Inert atmosphere

With sodium cyanoborohydride; trifluoroacetic acid; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; 1,2-dichloro-ethane;
DOI:10.1016/j.bmcl.2011.09.057