N-Anthraquinonyl-1-anthranilic acid

Base Information

• Chemical Name: N-Anthraquinonyl-1-anthranilic acid
• CAS No.: 19795-96-1
• Molecular Formula: C21H13 N O4
• Molecular Weight: 343.339
• Hs Code.: 2922509090
• European Community (EC) Number: 243-320-8
• UNII: 470TN2GY8F
• DSSTox Substance ID: DTXSID40173505
• Nikkaji Number: J225.281C
• Wikidata: Q27258978
• ChEMBL ID: CHEMBL1530154
• Mol file: 19795-96-1.mol

Synonyms:N-Anthraquinonyl-1-anthranilic acid;19795-96-1;UNII-470TN2GY8F;470TN2GY8F;2-[(9,10-DIHYDRO-9,10-DIOXO-1-ANTHRYL)AMINO]BENZOIC ACID;2-[(9,10-dioxoanthracen-1-yl)amino]benzoic acid;EINECS 243-320-8;2-((9,10-Dihydro-9,10-dioxo-1-anthryl)amino)benzoic acid;2-[(9,10-dioxo-9,10-dihydroanthracen-1-yl)amino]benzoic acid;Benzoic acid, 2-((9,10-dihydro-9,10-dioxo-1-anthracenyl)amino)-;2-((9,10-Dioxo-9,10-dihydroanthracen-1-yl)amino)benzoic acid;Benzoic acid,2-[(9,10-dihydro-9,10-dioxo-1-anthracenyl)amino]-;SOLVENT VIOLET 60;SCHEMBL8444248;CHEMBL1530154;DTXSID40173505;STK238453;AKOS000592940;2-(1-anthraquinonylamino)-benzoic acid;CS-0336596;EU-0000455;UNM000011032701;2-(1-ANTHRAQUINONYLAMINO)BENZOIC ACID;ANTHRANILIC ACID, N-1-ANTHRAQUINONYL-;C.I. 605120;W-110501;Q27258978;2-[(9,10-Dihydro-9,10-dioxoanthracen-1-yl)amino]benzoic acid;2-[(9,10-dioxo-9,10-dihydro-1-anthracenyl)amino]benzoic acid;ANTHRANILIC ACID, N-(9,10-DIHYDRO-9,10-DIOXO-1-ANTHRYL)-

Chemical Property of N-Anthraquinonyl-1-anthranilic acid

Chemical Property:

• Vapor Pressure: 5.45E-14mmHg at 25°C
• Boiling Point: 573.4°Cat760mmHg
• Flash Point: 300.6°C
• PSA: 83.47000
• Density: 1.444g/cm³
• LogP: 3.97680
• XLogP3: 4.5
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 3
• Exact Mass: 343.08445790
• Heavy Atom Count: 26
• Complexity: 589

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(C2=O)C(=CC=C3)NC4=CC=CC=C4C(=O)O

Technology Process of N-Anthraquinonyl-1-anthranilic acid

There total 5 articles about N-Anthraquinonyl-1-anthranilic acid 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:

1-chloroanthracene-9,10-dione (82-44-0) + anthranilic acid (118-92-3,159201-01-1,50816-84-7,80206-34-4,104809-47-4) → 1-anilido-o-carboxy-9,10-anthracene-dione (19795-96-1)

Guidance literature:

With potassium acetate; copper (I) acetate; copper; at 150 - 160 ℃; weiteres Reagens: Isoamylalkohol;

Reference yield:

1-amino-9,10-anthracenedione (82-45-1) + ortho-chlorobenzoic acid (118-91-2) → 1-anilido-o-carboxy-9,10-anthracene-dione (19795-96-1)

Guidance literature:

With copper; sodium carbonate; nitrobenzene; at 220 - 230 ℃;

Reference yield:

1-anthraquinonesulfonic acid (82-49-5) → 1-anilido-o-carboxy-9,10-anthracene-dione (19795-96-1)

Guidance literature:

Multi-step reaction with 2 steps

1: hydrochloric acid; aqueous-sodium chlorate

2: potassium acetate; copper acetate; copper powder / 150 - 160 °C / weiteres Reagens: Isoamylalkohol

With hydrogenchloride; sodium chlorate; potassium acetate; copper (I) acetate; copper;

upstream raw materials:

1-amino-9,10-anthracenedione

ortho-chlorobenzoic acid

1-nitroanthraquinone

anthranilic acid

Downstream raw materials:

13H-Naphtho[2,3-c]acridine-5,8,14-trione

6,10,12-trichloro-13H-naphth[2,3-c]acridine-5,8,14-trione