N-(1-Methoxyethyl)benzamide

Base Information

Chemical Name:N-(1-Methoxyethyl)benzamide
CAS No.:115245-46-0
Molecular Formula:C10H13 N O2
Molecular Weight:179.219
Hs Code.:
DSSTox Substance ID:DTXSID70550623
Mol file:115245-46-0.mol

Synonyms:N-(1-Methoxyethyl)benzamide;115245-46-0;Benzamide, N-(1-methoxyethyl)-;DTXSID70550623

Suppliers and Price of N-(1-Methoxyethyl)benzamide

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 N-(1-Methoxyethyl)benzamide

Chemical Property:

PSA：41.82000
LogP:1.98360
XLogP3:1.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:179.094628657
Heavy Atom Count:13
Complexity:164

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(NC(=O)C1=CC=CC=C1)OC

Technology Process of N-(1-Methoxyethyl)benzamide

There total 2 articles about N-(1-Methoxyethyl)benzamide 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: 100.0%

: 67-56-1
methanol

: 2198-64-3,1205-02-3,90988-29-7
N-Benzoylalanine

: 115245-46-0
N-(1-methoxyethyl)benzamide

Guidance literature:: With piperidine; silica gel; at 0 ℃; Electrolysis;
DOI:10.1021/ja070283w

Reference yield:

: 67-56-1
methanol

: 1575-95-7
N-acetylbenzamide

: 115245-46-0
N-(1-methoxyethyl)benzamide

Guidance literature:: With 3-(1-piperidino)propyl functionalized silica gel (SiO₂-Pip); at 10 ℃; Electrochemical reaction;
DOI:10.1016/j.tet.2018.12.042