4-(2-aminobenzoyl)-1,3-dihydro-2H-Imidazol-2-one

Base Information

Chemical Name:4-(2-aminobenzoyl)-1,3-dihydro-2H-Imidazol-2-one
CAS No.:849454-36-0
Molecular Formula:C10H9 N3 O2
Molecular Weight:203.2
Hs Code.:
DSSTox Substance ID:DTXSID10699101
Wikidata:Q82629839

Synonyms:4-(2-aminobenzoyl)-1,3-dihydro-2H-Imidazol-2-one;DTXSID10699101;FT-0732154

Suppliers and Price of 4-(2-aminobenzoyl)-1,3-dihydro-2H-Imidazol-2-one

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 4 raw suppliers

Chemical Property of 4-(2-aminobenzoyl)-1,3-dihydro-2H-Imidazol-2-one

Chemical Property:

XLogP3:0.6
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:203.069476538
Heavy Atom Count:15
Complexity:325

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C(=C1)C(=O)C2=CNC(=O)N2)N

Technology Process of 4-(2-aminobenzoyl)-1,3-dihydro-2H-Imidazol-2-one

There total 2 articles about 4-(2-aminobenzoyl)-1,3-dihydro-2H-Imidazol-2-one 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: 98.0%

: 849454-35-9
4-nitrobenzoyl-1,3-dihydroimidazol-2-one

: 849454-36-0
4-aminobenzoyl-1,3-dihydroimidazol-2-one

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol;
DOI:10.1016/j.bmcl.2007.02.076

Reference yield:

: 610-14-0
2-nitrobenzyl chloride

: 849454-36-0
4-aminobenzoyl-1,3-dihydroimidazol-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 45 percent / AlCl₃ / nitrobenzene

2: 98 percent / H₂ / Pd/C / methanol

With aluminium trichloride; hydrogen; palladium on activated charcoal; In methanol; nitrobenzene; 1: Friedel-Crafts acylation;
DOI:10.1016/j.bmcl.2007.02.076

Reference yield: 6.4%

: 362488-51-5
4-[(2-methyl-4-quinolinyl)methoxy]-benzoic acid

: 849454-36-0
4-aminobenzoyl-1,3-dihydroimidazol-2-one

: 4-(2-methyl-quinolin-4-ylmethoxy)-N-[2-(2-oxo-2,3-dihydro-1H-imidazole-4-carbonyl)phenyl]benzamide trifluoroacetate

Guidance literature:: 4-[(2-methyl-4-quinolinyl)methoxy]-benzoic acid; With pyridine; trichlorophosphate; for 0.25h;

4-aminobenzoyl-1,3-dihydroimidazol-2-one; for 1h;

With dmap; at 20 ℃;