Benzeneacetamide, N-(2-hydroxy-1,1-dimethylethyl)-

Base Information

Chemical Name:Benzeneacetamide, N-(2-hydroxy-1,1-dimethylethyl)-
CAS No.:1569-06-8
Molecular Formula:C12H17NO2
Molecular Weight:207.272
Hs Code.:
DSSTox Substance ID:DTXSID30473768
Wikidata:Q82303386
Mol file:1569-06-8.mol

Synonyms:Benzeneacetamide, N-(2-hydroxy-1,1-dimethylethyl)-;1569-06-8;SCHEMBL6188972;DTXSID30473768;AKOS008975611

Suppliers and Price of Benzeneacetamide, N-(2-hydroxy-1,1-dimethylethyl)-

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
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price

Total 1 raw suppliers

Chemical Property of Benzeneacetamide, N-(2-hydroxy-1,1-dimethylethyl)-

Chemical Property:

XLogP3:1.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:207.125928785
Heavy Atom Count:15
Complexity:208

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(CO)NC(=O)CC1=CC=CC=C1

Technology Process of Benzeneacetamide, N-(2-hydroxy-1,1-dimethylethyl)-

There total 5 articles about Benzeneacetamide, N-(2-hydroxy-1,1-dimethylethyl)- 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: 95.0%

: 124-68-5
2-Amino-2-methyl-1-propanol

: 101-97-3
Ethyl 2-phenylethanoate

: 1569-06-8
N-(2-hydroxyl-1,1-dimethylethyl) benzeneamide

Guidance literature:: 2-Amino-2-methyl-1-propanol; With n-butyllithium; lanthanum(III) chloride; In dichloromethane; at 0 ℃; after the reagent addition stirring for 15 min at this temperature under nitrogen, than warming to reflux;

Ethyl 2-phenylethanoate; for 12h; reflux;
DOI:10.1080/00397919808004440