2,2-Dimethylbicyclo[3.2.1]oct-6-en-3-one

Base Information

Chemical Name:2,2-Dimethylbicyclo[3.2.1]oct-6-en-3-one
CAS No.:22940-29-0
Molecular Formula:C10H14O
Molecular Weight:150.221
Hs Code.:
DSSTox Substance ID:DTXSID90499848
Mol file:22940-29-0.mol

Synonyms:22940-29-0;2,2-Dimethylbicyclo[3.2.1]oct-6-en-3-one;DTXSID90499848

Suppliers and Price of 2,2-Dimethylbicyclo[3.2.1]oct-6-en-3-one

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 2,2-Dimethylbicyclo[3.2.1]oct-6-en-3-one

Chemical Property:

XLogP3:1.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:150.104465066
Heavy Atom Count:11
Complexity:225

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1(C2CC(CC1=O)C=C2)C

Technology Process of 2,2-Dimethylbicyclo[3.2.1]oct-6-en-3-one

There total 1 articles about 2,2-Dimethylbicyclo[3.2.1]oct-6-en-3-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:

: 1111-97-3
3-chloro-3-methylbut-1-yne

: 542-92-7,25568-84-7,7313-32-8
cyclopenta-1,3-diene

: 22940-29-0
2,2-dimethylbicyclo<3.2.1>oct-6-en-3-one

: 65404-99-1
3-Chlor-4,4-dimethylbicyclo<3.2.1>octa-2,6-dien

: 344257-36-9
4-(1,1-Dimethyl-2-propinyl)-2-cyclopenten-1-ol

: 107-19-7
propargyl alcohol

: 115-19-5
2-methyl-but-3-yn-2-ol

Guidance literature:: With potassium hydroxide; silver trifluoroacetate; In pentane; at 0 ℃; Mechanism;

Reference yield: 49.0%

: 22940-29-0
2,2-dimethylbicyclo<3.2.1>oct-6-en-3-one

: 100-52-7
benzaldehyde

: (1RS,5SR,4E)-4-benzylidene-2,2-dimethylbicyclo<3.2.1>oct-6-en-3-one

: (1RS,4RS,5SR,1'RS)-4-(1'-hydroxybenzyl)-2,2-dimethylbicyclo<3.2.1>oct-6-en-3-one

Guidance literature:: With lithium diisopropyl amide; In tetrahydrofuran; hexane; at 0 ℃; for 0.5h;
DOI:10.1002/hlca.19930760604

Reference yield:

: 22940-29-0
2,2-dimethylbicyclo<3.2.1>oct-6-en-3-one

: (1RS,4RS,5SR,1'RS)-4-<1'-(4-bromophenylsulfonyloxy)ethyl>-2,2-dimethylbicyclo<3.2.1>oct-6-en-3-one

Guidance literature:: Multi-step reaction with 2 steps

1: 74 percent / lithium diisopropylamide / hexane; tetrahydrofuran / 0.5 h / -20 °C

2: 72 percent / lithium diisopropylamide / tetrahydrofuran / 1 h / Ambient temperature

With lithium diisopropyl amide; In tetrahydrofuran; hexane;
DOI:10.1002/hlca.19930760604