2-Oxo-3-phenoxy-N,N-di(propan-2-yl)propanamide

Base Information

Chemical Name:2-Oxo-3-phenoxy-N,N-di(propan-2-yl)propanamide
CAS No.:120313-14-6
Molecular Formula:C15H21NO3
Molecular Weight:263.337
Hs Code.:
DSSTox Substance ID:DTXSID30559056
Nikkaji Number:J2.019.153H
Wikidata:Q82441584

Synonyms:120313-14-6;2-Oxo-3-phenoxy-N,N-di(propan-2-yl)propanamide;DTXSID30559056

Suppliers and Price of 2-Oxo-3-phenoxy-N,N-di(propan-2-yl)propanamide

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 2-Oxo-3-phenoxy-N,N-di(propan-2-yl)propanamide

Chemical Property:

XLogP3:2.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:263.15214353
Heavy Atom Count:19
Complexity:299

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)N(C(C)C)C(=O)C(=O)COC1=CC=CC=C1

Technology Process of 2-Oxo-3-phenoxy-N,N-di(propan-2-yl)propanamide

There total 1 articles about 2-Oxo-3-phenoxy-N,N-di(propan-2-yl)propanamide 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: 30.0%

: 120313-13-5
ethyl 2-(diisopropylamino)-2-oxoacetate

: 122-59-8
2-phenoxyacetic acid

: 120313-14-6
N,N-diisopropyl-2-oxo-3-phenoxypropanamide

Guidance literature:: 2-phenoxyacetic acid; With lithium diisopropyl amide; In tetrahydrofuran; at -72 ℃;

ethyl 2-(diisopropylamino)-2-oxoacetate; With hydrogenchloride; In tetrahydrofuran;
DOI:10.1021/jo060338x