1-(2,6,6-Trimethyloxan-2-yl)ethan-1-one

Base Information

Chemical Name:1-(2,6,6-Trimethyloxan-2-yl)ethan-1-one
CAS No.:73410-33-0
Molecular Formula:C10H18O2
Molecular Weight:170.252
Hs Code.:
DSSTox Substance ID:DTXSID80532490

Synonyms:73410-33-0;1-(2,6,6-Trimethyloxan-2-yl)ethan-1-one;SCHEMBL15116543;DTXSID80532490

Suppliers and Price of 1-(2,6,6-Trimethyloxan-2-yl)ethan-1-one

Supply Marketing:

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

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Chemical Property of 1-(2,6,6-Trimethyloxan-2-yl)ethan-1-one

Chemical Property:

XLogP3:1.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:170.130679813
Heavy Atom Count:12
Complexity:196

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)C1(CCCC(O1)(C)C)C

Technology Process of 1-(2,6,6-Trimethyloxan-2-yl)ethan-1-one

There total 1 articles about 1-(2,6,6-Trimethyloxan-2-yl)ethan-1-one 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: 24.0%

: 917-64-6
methyl magnesium iodide

: 88974-48-5
1,5-dimethyl-6,8-dioxabicyclo[3.2.1]octan-7-one

: 73410-33-0
1-(2,6,6-Trimethyl-tetrahydro-pyran-2-yl)-ethanone

: 470-59-7
tetrahydro-2,6,6-trimethyl-2H-pyran-2-carboxylic acid

Guidance literature:: In diethyl ether; for 7h; Ambient temperature;
DOI:10.1016/S0040-4039(00)81983-8

Reference yield:

: 73410-33-0
1-(2,6,6-Trimethyl-tetrahydro-pyran-2-yl)-ethanone

: 7392-19-0,13226-34-1,13837-56-4
2-vinyl-2,6,6-trimethyl-3,4,5,6-tetrahydro-2H-pyran

Guidance literature:: Multi-step reaction with 3 steps

1: LiAlH₄

2: 1.) NaH

3: Heating

With lithium aluminium tetrahydride; sodium hydride;