Benzamide, 2-(methylamino)-N-2-propenyl-

Base Information

Chemical Name:Benzamide, 2-(methylamino)-N-2-propenyl-
CAS No.:68614-89-1
Molecular Formula:C₁₁H₁₄N₂O
Molecular Weight:190.245
Hs Code.:
DSSTox Substance ID:DTXSID80399247
Wikidata:Q82201661

Synonyms:68614-89-1;Benzamide, 2-(methylamino)-N-2-propenyl-;DTXSID80399247;AKOS009053007

Suppliers and Price of Benzamide, 2-(methylamino)-N-2-propenyl-

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 Benzamide, 2-(methylamino)-N-2-propenyl-

Chemical Property:

XLogP3:2.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:190.110613074
Heavy Atom Count:14
Complexity:204

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CNC1=CC=CC=C1C(=O)NCC=C

Technology Process of Benzamide, 2-(methylamino)-N-2-propenyl-

There total 3 articles about Benzamide, 2-(methylamino)-N-2-propenyl- 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: 70.0%

: 4943-82-2
N-allyl-2-aminobenzamide

: 74-88-4
methyl iodide

: 68614-89-1
N-allyl-2-methylaminobenzamide

Guidance literature:: With potassium carbonate; In acetonitrile; for 8h; Reflux;
DOI:10.1039/c5ra23013f

Reference yield:

: 118-92-3,159201-01-1,50816-84-7,80206-34-4,104809-47-4
anthranilic acid

: 68614-89-1
N-allyl-2-methylaminobenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / dichloromethane / 12 h / 0 - 20 °C

2: potassium carbonate / acetonitrile / 8 h / Reflux

With dmap; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; acetonitrile;
DOI:10.1039/c5ra23013f