4-(2-(1H-imidazol-1-yl)ethoxy)benzamide

Base Information

Chemical Name:4-(2-(1H-imidazol-1-yl)ethoxy)benzamide
CAS No.:75912-57-1
Molecular Formula:C₁₂H₁₃N₃O₂
Molecular Weight:231.254
Hs Code.:
UNII:X4KD3DE9YZ
ChEMBL ID:CHEMBL30395
Pharos Ligand ID:BYR6AK1D8UVR

Synonyms:4-(2-(1H-imidazol-1-yl)ethoxy)benzamide;X4KD3DE9YZ;CHEMBL30395;75912-57-1;4-(2-imidazol-1-ylethoxy)benzamide;Benzamide, 4-(2-(1H-imidazol-1-yl)ethoxy)-;4-(2-Imidazol-1-yl-ethoxy)-benzamide;UNII-X4KD3DE9YZ;SCHEMBL3005716;DVALIYTWWUIPGC-UHFFFAOYSA-N;BDBM50025995;PD181637;1-[2-(4-carbamoylphenoxy)ethyl]imidazole;1-[2-(4-carbamoyl phenoxy)ethyl]imidazole

Suppliers and Price of 4-(2-(1H-imidazol-1-yl)ethoxy)benzamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 4-(2-(1H-imidazol-1-yl)ethoxy)benzamide

Chemical Property:

XLogP3:0.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:231.100776666
Heavy Atom Count:17
Complexity:252

Purity/Quality:

Safty Information:

Pictogram(s):
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MSDS Files:

Useful:

Canonical SMILES:C1=CC(=CC=C1C(=O)N)OCCN2C=CN=C2

Technology Process of 4-(2-(1H-imidazol-1-yl)ethoxy)benzamide

There total 1 articles about 4-(2-(1H-imidazol-1-yl)ethoxy)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:

: 288-32-4
1H-imidazole

: 36616-30-5
2-(4-carbamoylphenoxy)-ethyl chloride

: 75912-57-1
4-<2-(1H-imidazol-1-yl)ethoxy>benzamide

Guidance literature:: With sodium hydride; Yield given. Multistep reaction; 1.) DMF, 100 deg C, 10 min, 2.) DMF, heating, 5.5 h;
DOI:10.1021/jm00148a009