Benzamide, N-(4-(1-methyl-2-(((1-methylethyl)sulfonyl)amino)ethyl)phenyl)-

Base Information

Chemical Name:Benzamide, N-(4-(1-methyl-2-(((1-methylethyl)sulfonyl)amino)ethyl)phenyl)-
CAS No.:211313-51-8
Molecular Formula:C₁₉H₂₄N₂O₃S
Molecular Weight:360.477
Hs Code.:
UNII:U9AF5D17SA
Nikkaji Number:J1.553.118E
Wikidata:Q27116279
Pharos Ligand ID:SC1FNWQGDLAU
ChEMBL ID:CHEMBL105076

Synonyms:LY-395153;211313-51-8;U9AF5D17SA;Benzamide, N-(4-(1-methyl-2-(((1-methylethyl)sulfonyl)amino)ethyl)phenyl)-;UNII-U9AF5D17SA;LY395153;CHEMBL105076;CHEBI:34809;N-{4-[1-Methyl-2-(propane-2-sulfonylamino)-ethyl]-phenyl}-benzamide;N-[4-[1-(propan-2-ylsulfonylamino)propan-2-yl]phenyl]benzamide;BDBM50102263;AKOS040748853;Q27116279

Suppliers and Price of Benzamide, N-(4-(1-methyl-2-(((1-methylethyl)sulfonyl)amino)ethyl)phenyl)-

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 Benzamide, N-(4-(1-methyl-2-(((1-methylethyl)sulfonyl)amino)ethyl)phenyl)-

Chemical Property:

XLogP3:3.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:7
Exact Mass:360.15076381
Heavy Atom Count:25
Complexity:513

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)S(=O)(=O)NCC(C)C1=CC=C(C=C1)NC(=O)C2=CC=CC=C2

Technology Process of Benzamide, N-(4-(1-methyl-2-(((1-methylethyl)sulfonyl)amino)ethyl)phenyl)-

There total 3 articles about Benzamide, N-(4-(1-methyl-2-(((1-methylethyl)sulfonyl)amino)ethyl)phenyl)- 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: 74.0%

: 98-88-4
benzoyl chloride

: 211315-28-5
N-[2-(4-aminophenyl)propyl]propane-2-sulfonamide

: 211313-51-8
LY₃₉₅₁₅₃

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 3h;
DOI:10.1021/jm000462n

Reference yield:

: 211315-27-4
N-2-(4-(N',N'-dibenzylamino)phenyl)propyl 2-propanesulfonamide

: 211313-51-8
LY₃₉₅₁₅₃

Guidance literature:: Multi-step reaction with 2 steps

1: 93 percent / ammonium formate; H₂ / 10percent Pd/C / ethanol / 6 h / 25 °C

2: 74 percent / Et₃N / CH₂Cl₂ / 3 h / 20 °C

With hydrogen; ammonium formate; triethylamine; 10percent Pd/C; In ethanol; dichloromethane;
DOI:10.1021/jm000462n

Reference yield:

: 2-(4-(N,N-dibenzylamino)phenyl)propylamine hydrochloride

: 211313-51-8
LY₃₉₅₁₅₃

Guidance literature:: Multi-step reaction with 3 steps

1: 63 percent / triethylamine / CH₂Cl₂ / 7 h / 0 - 20 °C

2: 93 percent / ammonium formate; H₂ / 10percent Pd/C / ethanol / 6 h / 25 °C

3: 74 percent / Et₃N / CH₂Cl₂ / 3 h / 20 °C

With hydrogen; ammonium formate; triethylamine; 10percent Pd/C; In ethanol; dichloromethane;
DOI:10.1021/jm000462n