3(4H)-Quinazolineacetamide, N-(2-nitrophenyl)-4-oxo-

Base Information

Chemical Name:3(4H)-Quinazolineacetamide, N-(2-nitrophenyl)-4-oxo-
CAS No.:108086-42-6
Molecular Formula:C₁₆H₁₂N₄O₄
Molecular Weight:324.296
Hs Code.:
DSSTox Substance ID:DTXSID60148376
Wikidata:Q83013888

Synonyms:BRN 5622233;3(4H)-Quinazolineacetamide, N-(2-nitrophenyl)-4-oxo-;N-(2-Nitrophenyl)-4-oxo-3(4H)-quinazolineacetamide;108086-42-6;CBKinase1_006285;CBKinase1_018685;DTXSID60148376;STK793241;AKOS001754775;LS-139953;BRD-K64352268-001-01-8;N-(2-nitrophenyl)-2-(4-oxoquinazolin-3(4H)-yl)acetamide;N~1~-(2-nitrophenyl)-2-[4-oxo-3(4H)-quinazolinyl]acetamide

Suppliers and Price of 3(4H)-Quinazolineacetamide, N-(2-nitrophenyl)-4-oxo-

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 0 raw suppliers

Chemical Property of 3(4H)-Quinazolineacetamide, N-(2-nitrophenyl)-4-oxo-

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.44g/cm³
XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:324.08585488
Heavy Atom Count:24
Complexity:545

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C(=O)N(C=N2)CC(=O)NC3=CC=CC=C3[N+](=O)[O-]

Technology Process of 3(4H)-Quinazolineacetamide, N-(2-nitrophenyl)-4-oxo-

There total 2 articles about 3(4H)-Quinazolineacetamide, N-(2-nitrophenyl)-4-oxo- 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%

: 10147-70-3
2-chloro-N-(2-nitrophenyl)acetamide

: 491-36-1
4-Hydroxyquinazoline

: 108086-42-6
N-(2-Nitro-phenyl)-2-(4-oxo-4H-quinazolin-3-yl)-acetamide

Guidance literature:: With pyridine; for 2h; Heating;

Reference yield:

: 88-74-4
2-nitro-aniline

: 108086-42-6
N-(2-Nitro-phenyl)-2-(4-oxo-4H-quinazolin-3-yl)-acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: 55 percent / benzene / 5 h / Heating

2: 70 percent / pyridine / 2 h / Heating

With pyridine; In benzene;