4-Benzylidene-1-(benzylideneamino)-2-phenyl-2-imidazolin-5-one

Base Information

Chemical Name:4-Benzylidene-1-(benzylideneamino)-2-phenyl-2-imidazolin-5-one
CAS No.:102546-05-4
Molecular Formula:C23H17 N3 O
Molecular Weight:351.407
Hs Code.:
Mol file:102546-05-4.mol

Synonyms:4-Benzylidene-1-(benzylideneamino)-2-phenyl-2-imidazolin-5-one;2-Imidazolin-5-one, 4-benzylidene-1-(benzylideneamino)-2-phenyl-;4H-Imidazol-4-one, 3,5-dihydro-2-phenyl-5-(phenylmethylene)-3-((phenylmethylene)amino)-;102546-05-4;CCG-42744;LS-79982;SR-01000632719-1;(5Z)-5-benzylidene-3-[(E)-benzylideneamino]-2-phenylimidazol-4-one

Suppliers and Price of 4-Benzylidene-1-(benzylideneamino)-2-phenyl-2-imidazolin-5-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
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price

Total 1 raw suppliers

Chemical Property of 4-Benzylidene-1-(benzylideneamino)-2-phenyl-2-imidazolin-5-one

Chemical Property:

XLogP3:4.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:351.137162174
Heavy Atom Count:27
Complexity:603

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C=C2C(=O)N(C(=N2)C3=CC=CC=C3)N=CC4=CC=CC=C4
Isomeric SMILES:C1=CC=C(C=C1)/C=C\2/C(=O)N(C(=N2)C3=CC=CC=C3)/N=C/C4=CC=CC=C4

Technology Process of 4-Benzylidene-1-(benzylideneamino)-2-phenyl-2-imidazolin-5-one

There total 4 articles about 4-Benzylidene-1-(benzylideneamino)-2-phenyl-2-imidazolin-5-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: 81.0%

: 1466-97-3
2-(benzamido)-N'-benzylidene-3-phenylacrylohydrazide

: 102546-05-4
4-(benzylidene)-1-(benzylideneamino)-2-phenyl-1H-imidazol-5(4H)-one

Guidance literature:: With trichlorophosphate; In chloroform; at 40 ℃; for 2h;

Reference yield:

: 842-74-0,5839-91-8
4-benzylidene-2-phenyloxazole-5(4H)-one

: 102546-05-4
4-(benzylidene)-1-(benzylideneamino)-2-phenyl-1H-imidazol-5(4H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: 62 percent / hydrazine hydrate / ethanol / Heating

2: 84 percent / glacial acetic acid / ethanol / 2 h / Heating

3: 81 percent / POCl₃ / CHCl₃ / 2 h / 40 °C

With hydrazine hydrate; acetic acid; trichlorophosphate; In ethanol; chloroform;

Reference yield:

: 40108-63-2
N-(3-hydrazinyl-3-oxo-1-phenylprop-1-en-2-yl)benzamide

: 102546-05-4
4-(benzylidene)-1-(benzylideneamino)-2-phenyl-1H-imidazol-5(4H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: 84 percent / glacial acetic acid / ethanol / 2 h / Heating

2: 81 percent / POCl₃ / CHCl₃ / 2 h / 40 °C

With acetic acid; trichlorophosphate; In ethanol; chloroform;