(4-tert-Butylpiperidin-1-yl)[2,4,6-tri(propan-2-yl)phenyl]methanone

Base Information

Chemical Name:(4-tert-Butylpiperidin-1-yl)[2,4,6-tri(propan-2-yl)phenyl]methanone
CAS No.:79288-68-9
Molecular Formula:C25H41NO
Molecular Weight:371.607
Hs Code.:
DSSTox Substance ID:DTXSID70508280
Wikidata:Q82365061

Synonyms:79288-68-9;DTXSID70508280;(4-tert-Butylpiperidin-1-yl)[2,4,6-tri(propan-2-yl)phenyl]methanone

Suppliers and Price of (4-tert-Butylpiperidin-1-yl)[2,4,6-tri(propan-2-yl)phenyl]methanone

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 1 raw suppliers

Chemical Property of (4-tert-Butylpiperidin-1-yl)[2,4,6-tri(propan-2-yl)phenyl]methanone

Chemical Property:

XLogP3:7.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:5
Exact Mass:371.318814931
Heavy Atom Count:27
Complexity:461

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)C1=CC(=C(C(=C1)C(C)C)C(=O)N2CCC(CC2)C(C)(C)C)C(C)C

Technology Process of (4-tert-Butylpiperidin-1-yl)[2,4,6-tri(propan-2-yl)phenyl]methanone

There total 2 articles about (4-tert-Butylpiperidin-1-yl)[2,4,6-tri(propan-2-yl)phenyl]methanone 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:

: 49623-71-4
2,4,6-triisopropylbenzoic acid

: 79288-68-9
4-tert-butyl-2,4,6-triisopropylbenzopiperidide

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / 12 h / Heating

2: diethyl ether

With thionyl chloride; In diethyl ether;
DOI:10.1021/ja00316a033