2,9-Diaminoacridine

Base Information

• Chemical Name: 2,9-Diaminoacridine
• CAS No.: 23043-62-1
• Molecular Formula: C13H11 N3
• Molecular Weight: 209.25
• Hs Code.: 2933990090
• DSSTox Substance ID: DTXSID80177603
• Nikkaji Number: J88.114G
• Wikidata: Q83047918
• Mol file: 23043-62-1.mol

Synonyms:2,9-Diaminoacridine;2,9-Acridinediamine;CCRIS 2109;ACRIDINE, 2,9-DIAMINO-;23043-62-1;BRN 0173190;4-22-00-06503 (Beilstein Handbook Reference);2,9-Diaminoacridin;SCHEMBL4154837;DTXSID80177603;FCXMXTMQASDIDU-UHFFFAOYSA-N;LS-14309

Chemical Property of 2,9-Diaminoacridine

Chemical Property:

• Vapor Pressure: 7.06E-10mmHg at 25°C
• Boiling Point: 493.4°Cat760mmHg
• Flash Point: 284.3°C
• PSA: 65.66000
• Density: 1.346g/cm³
• LogP: 3.06370
• XLogP3: 1.9
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 0
• Exact Mass: 209.095297364
• Heavy Atom Count: 16
• Complexity: 256

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C2C(=C1)C(=C3C=C(C=CC3=N2)N)N

Technology Process of 2,9-Diaminoacridine

There total 1 articles about 2,9-Diaminoacridine 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:

2-aminoacridone (27918-14-5) → 2,9-diamino-acridine (23043-62-1)

Guidance literature:

Multi-step reaction with 3 steps

1: ethanol

2: POCl₃

3: 4>2CO₃; phenol

With ethanol; ammonium carbonate; trichlorophosphate; phenol;

DOI:10.1039/jr9490001148

Reference yield:

2,9-diamino-acridine (23043-62-1) → 9-amino-2-azidoacridine (78276-18-3)

Guidance literature:

With sodium nitrate; sodium azide; Yield given. Multistep reaction; 1.) 5 min;

DOI:10.1021/jm00373a010

upstream raw materials:

2-aminoacridone

Downstream raw materials:

9-amino-2-azidoacridine