2-(4-Oxo-2,3-diphenylindeno[1,2-b]pyrrol-1(4H)-yl)ethyl acetate

Base Information

Chemical Name:2-(4-Oxo-2,3-diphenylindeno[1,2-b]pyrrol-1(4H)-yl)ethyl acetate
CAS No.:105772-24-5
Molecular Formula:C₂₇H₂₁NO₃
Molecular Weight:407.469
Hs Code.:
DSSTox Substance ID:DTXSID00559821
Wikidata:Q82442670

Synonyms:105772-24-5;2-(4-Oxo-2,3-diphenylindeno[1,2-b]pyrrol-1(4H)-yl)ethyl acetate;DTXSID00559821

Suppliers and Price of 2-(4-Oxo-2,3-diphenylindeno[1,2-b]pyrrol-1(4H)-yl)ethyl acetate

Supply Marketing:

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

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Chemical Property of 2-(4-Oxo-2,3-diphenylindeno[1,2-b]pyrrol-1(4H)-yl)ethyl acetate

Chemical Property:

XLogP3:4.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:407.15214353
Heavy Atom Count:31
Complexity:651

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)OCCN1C(=C(C2=C1C3=CC=CC=C3C2=O)C4=CC=CC=C4)C5=CC=CC=C5

Technology Process of 2-(4-Oxo-2,3-diphenylindeno[1,2-b]pyrrol-1(4H)-yl)ethyl acetate

There total 3 articles about 2-(4-Oxo-2,3-diphenylindeno[1,2-b]pyrrol-1(4H)-yl)ethyl acetate 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: 70.0%

: 86489-62-5
2-desylindan-1,3-dione

: 141-43-5
ethanolamine

: 105772-24-5
N-(β-acetoxyethyl)-2,3-diphenyl-4-oxoindeno<1,2-b>pyrrole

Guidance literature:: With acetic acid; for 12h; Heating;

Reference yield:

: 606-23-5
1H-indene-1,3(2H)-dione

: 105772-24-5
N-(β-acetoxyethyl)-2,3-diphenyl-4-oxoindeno<1,2-b>pyrrole

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) K₂CO₃ / 1.) CHCl₃, 1 h, 2.) 24 h

2: 70 percent / glacial acetic acid / 12 h / Heating

With potassium carbonate; acetic acid;

Reference yield:

: 447-31-4
Desyl chloride

: 105772-24-5
N-(β-acetoxyethyl)-2,3-diphenyl-4-oxoindeno<1,2-b>pyrrole

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) K₂CO₃ / 1.) CHCl₃, 1 h, 2.) 24 h

2: 70 percent / glacial acetic acid / 12 h / Heating

With potassium carbonate; acetic acid;