Naphth[2,3-c]acridine-5,8,14(13H)-trione, 6-amino-

Base Information

• Chemical Name: Naphth[2,3-c]acridine-5,8,14(13H)-trione, 6-amino-
• CAS No.: 81-73-2
• Molecular Formula: C21H12N2O3
• Molecular Weight: 340.338
• European Community (EC) Number: 201-373-4
• DSSTox Substance ID: DTXSID5058854
• Nikkaji Number: J192.593H
• Wikidata: Q81988554
• Mol file: 81-73-2.mol

Synonyms:81-73-2;EINECS 201-373-4;Naphth[2,3-c]acridine-5,8,14(13H)-trione, 6-amino-;Naphth(2,3-c)acridine-5,8,14(13H)-trione, 6-amino-;6-Aminonaphth[2,3-c]acridine-5,8,14(13H)-trione;6-Aminonaphth(2,3-c)acridine-5,8,14(13H)-trione;DTXSID5058854;SCHEMBL11135578;C21-H12-N2-O3;6-aminonaphth[2,3-c]acridin-5,8,14(13H)-trion

Chemical Property of Naphth[2,3-c]acridine-5,8,14(13H)-trione, 6-amino-

Chemical Property:

• Vapor Pressure: 6.49E-18mmHg at 25°C
• Boiling Point: 671.9°Cat760mmHg
• Flash Point: 360.1°C
• PSA: 93.02000
• Density: 1.476g/cm³
• LogP: 3.62010
• XLogP3: 3.8
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 0
• Exact Mass: 340.08479225
• Heavy Atom Count: 26
• Complexity: 647

Purity/Quality:

99%, ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C2C(=C1)C(=O)C3=C(C=C4C(=C3C2=O)NC5=CC=CC=C5C4=O)N
• Use Description: 6-aminonaphth[2,3-c]acridine-5,8,14(13H)-trione, a chemical compound with a complex structure, has potential applications in various fields. In the pharmaceutical industry, it may serve as a scaffold or intermediate for the synthesis of pharmaceutical compounds, potentially contributing to drug development and manufacturing processes. Its unique chemical structure suggests it may be involved in creating drug candidates with specific pharmacological properties. Additionally, in the field of organic chemistry, it can be employed as a building block for the synthesis of complex organic molecules, aiding researchers in the development of new materials, catalysts, and specialty chemicals. While specific uses may vary depending on research and development needs, its primary significance likely lies in drug discovery and organic synthesis, making it a valuable tool for pharmaceutical researchers and chemists.

Technology Process of Naphth[2,3-c]acridine-5,8,14(13H)-trione, 6-amino-

There total 5 articles about Naphth[2,3-c]acridine-5,8,14(13H)-trione, 6-amino- 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:

N-(4-amino-9,10-dioxo-9,10-dihydro-[1]anthryl)-anthranilic acid (81-43-6) → 6-amino-13H-naphtho[2,3-c]acridine-5,8,14-trione (81-73-2)

Guidance literature:

With chlorosulfonic acid; at 35 - 40 ℃;

Reference yield:

→ 6-amino-13H-naphtho[2,3-c]acridine-5,8,14-trione (81-73-2)

Guidance literature:

With sulfuric acid;

Reference yield:

6-amino-7-chloro-13H-naphth[2,3-c]acridine-5,8,14-trione → 6-amino-13H-naphtho[2,3-c]acridine-5,8,14-trione (81-73-2)

Guidance literature:

With sodium hydroxide; sodium dithionite;

upstream raw materials:

N-(4-amino-9,10-dioxo-9,10-dihydro-[1]anthryl)-anthranilic acid

fluorosulphonic acid

N-(4-amino-3-chloro-9,10-dioxo-9,10-dihydro-[1]anthryl)-anthranilic acid