N-(1,3-dioxo-2-phenylbenzo[de]isoquinolin-6-yl)acetamide

Base Information

Chemical Name:N-(1,3-dioxo-2-phenylbenzo[de]isoquinolin-6-yl)acetamide
CAS No.:20119-29-3
Molecular Formula:C₂₀H₁₄N₂O₃
Molecular Weight:330.343
Hs Code.:
DSSTox Substance ID:DTXSID501152057
Nikkaji Number:J973.074E
ChEMBL ID:CHEMBL1454701
Mol file:20119-29-3.mol

Synonyms:N-(1,3-dioxo-2-phenyl-2,3-dihydro-1H-benzo[de]isoquinolin-6-yl)acetamide;Oprea1_273994;Oprea1_767818;MLS000712242;CHEMBL1454701;N-(1,3-dioxo-2-phenylbenzo[de]isoquinolin-6-yl)acetamide;DTXSID501152057;HMS2685E21;AKOS000635386;SMR000282009;AG-690/36720001;SR-01000313372;SR-01000313372-1;N-(2,3-Dihydro-1,3-dioxo-2-phenyl-1H-benz[de]isoquinolin-6-yl)acetamide;N-[(1,3-Dioxo-2-phenyl-2,3-dihydro-1H-benzo[de]isoquinoline)-6-yl]acetamide;20119-29-3

Suppliers and Price of N-(1,3-dioxo-2-phenylbenzo[de]isoquinolin-6-yl)acetamide

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of N-(1,3-dioxo-2-phenylbenzo[de]isoquinolin-6-yl)acetamide

Chemical Property:

XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:330.10044231
Heavy Atom Count:25
Complexity:569

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(=O)NC1=C2C=CC=C3C2=C(C=C1)C(=O)N(C3=O)C4=CC=CC=C4

Technology Process of N-(1,3-dioxo-2-phenylbenzo[de]isoquinolin-6-yl)acetamide

There total 7 articles about N-(1,3-dioxo-2-phenylbenzo[de]isoquinolin-6-yl)acetamide 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: 75.0%

: 10495-37-1
4-aminonaphthalic acid phenylimide

: 108-24-7
acetic anhydride

: 20119-29-3
4-(acetylamino)-N-phenyl-1,8-naphthalimide

Guidance literature:: With acetic acid; at 80 ℃; for 1.5h; Reflux;
DOI:10.1007/s11172-009-0160-x

Reference yield: 73.2%

: 26558-91-8
4-acetylaminonaphthalic-1,8-anhydride

: 62-53-3
aniline

: 20119-29-3
4-(acetylamino)-N-phenyl-1,8-naphthalimide

Guidance literature:: With acetic acid; for 10h; Heating;

Reference yield:

: 6642-29-1
4-nitronaphthalic-1,8-anhydride

: 20119-29-3
4-(acetylamino)-N-phenyl-1,8-naphthalimide

Guidance literature:: Multi-step reaction with 3 steps

1: acetic acid / 1.5 h / Reflux

2: hydrogenchloride; tin(II) chloride dihdyrate / ethanol; water / 1.5 h / 50 °C / Reflux

3: acetic acid / 1.5 h / 80 °C / Reflux

With hydrogenchloride; tin(II) chloride dihdyrate; acetic acid; In ethanol; water;
DOI:10.1007/s11172-009-0160-x