1-Propanone, 2,2-dimethyl-1-(1-naphthalenyl)-

Base Information

Chemical Name:1-Propanone, 2,2-dimethyl-1-(1-naphthalenyl)-
CAS No.:25540-73-2
Molecular Formula:C15H16O
Molecular Weight:212.291
Hs Code.:
DSSTox Substance ID:DTXSID70360885
Wikidata:Q82142903
Mol file:25540-73-2.mol

Synonyms:1-Propanone, 2,2-dimethyl-1-(1-naphthalenyl)-;25540-73-2;2,2-dimethyl-1-naphthalen-1-ylpropan-1-one;C15H16O;2,2-dimethyl-1-(1-naphthyl)-1-propanone;SCHEMBL8237885;DTXSID70360885;AKOS012009984;2,2-Dimethyl-1-naphthalen-1-yl-propan-1-one;AQ-917/42754498;2,2-DIMETHYL-1-(NAPHTHALEN-1-YL)PROPAN-1-ONE

Suppliers and Price of 1-Propanone, 2,2-dimethyl-1-(1-naphthalenyl)-

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

JR MediChem
2,2-DIMETHYL-1-(1-NAPHTHYL)-1-PROPANONE 96%
25g
$ 3980.00

JR MediChem
2,2-DIMETHYL-1-(1-NAPHTHYL)-1-PROPANONE 96%
5g
$ 1280.00

JR MediChem
2,2-DIMETHYL-1-(1-NAPHTHYL)-1-PROPANONE 96%
1g
$ 380.00

Total 0 raw suppliers

Chemical Property of 1-Propanone, 2,2-dimethyl-1-(1-naphthalenyl)-

Chemical Property:

PSA：17.07000
LogP:4.06860
XLogP3:4.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:212.120115130
Heavy Atom Count:16
Complexity:261

Purity/Quality:: 2,2-DIMETHYL-1-(1-NAPHTHYL)-1-PROPANONE 96% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)(C)C(=O)C1=CC=CC2=CC=CC=C21

Technology Process of 1-Propanone, 2,2-dimethyl-1-(1-naphthalenyl)-

There total 11 articles about 1-Propanone, 2,2-dimethyl-1-(1-naphthalenyl)- 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: 89.0%

: 90-11-9
1-Bromonaphthalene

: 3282-30-2
pivaloyl chloride

: 25540-73-2
1-pivaloylnaphthalene

Guidance literature:: 1-Bromonaphthalene; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 0.833333h; Schlenk technique; Inert atmosphere;

pivaloyl chloride; In tetrahydrofuran; hexane; at -78 - 20 ℃; for 2h; Schlenk technique; Inert atmosphere;
DOI:10.3762/bjoc.16.49