5-(2-fluorophenyl)-5H-imidazo[2,1-a]isoindole

Base Information

Chemical Name:5-(2-fluorophenyl)-5H-imidazo[2,1-a]isoindole
CAS No.:73268-33-4
Molecular Formula:C₁₆H₁₁FN₂
Molecular Weight:250.275
Hs Code.:
DSSTox Substance ID:DTXSID60512694
NSC Number:742548

Synonyms:73268-33-4;5-(2-fluorophenyl)-5H-imidazo[2,1-a]isoindole;SCHEMBL11458552;DTXSID60512694;NSC742548;5H-Imidazo[2, 5-(2-fluorophenyl)-;NSC-742548

Suppliers and Price of 5-(2-fluorophenyl)-5H-imidazo[2,1-a]isoindole

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 5-(2-fluorophenyl)-5H-imidazo[2,1-a]isoindole

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:250.09062652
Heavy Atom Count:19
Complexity:335

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C(N3C2=NC=C3)C4=CC=CC=C4F

Technology Process of 5-(2-fluorophenyl)-5H-imidazo[2,1-a]isoindole

There total 3 articles about 5-(2-fluorophenyl)-5H-imidazo[2,1-a]isoindole 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: 84.0%

: 81450-57-9
5-(2-Fluoro-phenyl)-2,5-dihydro-3H-imidazo[2,1-a]isoindol-5-ol

: 73268-33-4
5-(2'-fluorophenyl)-5H-imidazo[2,1-a]isoindole

Guidance literature:: In acetic acid; for 8h; Heating;
DOI:10.1002/jhet.5570180812

Reference yield:

: 936-49-2
2-phenyl-2-imidazoline

: 73268-33-4
5-(2'-fluorophenyl)-5H-imidazo[2,1-a]isoindole

Guidance literature:: Multi-step reaction with 2 steps

1: 1.)n-BuLi / 1.)THF/hexane, 50 deg C, 3 h 2.)r.t., overnight

2: 84 percent / acetic acid / 8 h / Heating

With n-butyllithium; In acetic acid;
DOI:10.1002/jhet.5570180812

Reference yield:

: 394-35-4
methyl 2-fluorobenzoate

: 73268-33-4
5-(2'-fluorophenyl)-5H-imidazo[2,1-a]isoindole

Guidance literature:: Multi-step reaction with 2 steps

1: 1.)n-BuLi / 1.)THF/hexane, 50 deg C, 3 h 2.)r.t., overnight

2: 84 percent / acetic acid / 8 h / Heating

With n-butyllithium; In acetic acid;
DOI:10.1002/jhet.5570180812