Ponsol Red Violet 2RNX

Base Information

• Chemical Name: Ponsol Red Violet 2RNX
• CAS No.: 6373-31-5
• Molecular Formula: C21H8 Cl3 N O3
• Molecular Weight: 428.658
• Hs Code.: 2933990090
• European Community (EC) Number: 228-916-8
• NSC Number: 47720
• DSSTox Substance ID: DTXSID80213151
• Nikkaji Number: J206.976H
• Wikidata: Q83088435
• Mol file: 6373-31-5.mol

Synonyms:Ponsol Red Violet 2RNX;C.I. Vat Violet 14;6373-31-5;Indanthrene Red Violet RRK;Vat Violet 14;Caledon Red Violet 2RN;Ponsol Red Violet RRNX;Ponsol Red Violet RRNXD;Benzadone Red Violet 2RK;Indanthren Red Violet RRK;Palanthrene Red Violet RRK;Carbanthrene Red Violet 2RNX;6,10,12-trichloro-13H-naphtho[2,3-c]acridine-5,8,14-trione;C.I. 67895;EINECS 228-916-8;NSC 47720;6,10,12-Trichloronaphth[2,3-c]acridine-5,8,14(13H)-trione;6,10,12-Trichloronaphth(2,3-c)acridine-5,8,14(13H)-trione;Naphth(2,3-c)acridine-5,8,14(13H)-trione, 6,10,12-trichloro-;Naphth(2,3-c)acridan-5,8,14-trione, 6,10,12-trichloro-;Naphth[2,3-c]acridan-5,8,14-trione, 6,10,12-trichloro-;Naphth[2,3-c]acridine-5,8,14(13H)-trione, 6,10,12-trichloro-;C21H8Cl3NO3;C21-H8-Cl3-N-O3;DTXSID80213151;NSC47720;NSC-47720;Naphth[2,8,14-trione, 6,10,12-trichloro-;Naphth[2,8,14(13H)-trione, 6,10,12-trichloro-;Naphtha(2,3-c)acridan-5,8,14-trione, 6,10,12-trichloro-

Chemical Property of Ponsol Red Violet 2RNX

Chemical Property:

• Vapor Pressure: 4.65E-18mmHg at 25°C
• Boiling Point: 674.6°C at 760 mmHg
• Flash Point: 361.8°C
• PSA: 67.00000
• Density: 1.623g/cm³
• LogP: 5.41690
• XLogP3: 5.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 426.956976
• Heavy Atom Count: 28
• Complexity: 715

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=C(C4=O)C=C(C=C5Cl)Cl)Cl

Technology Process of Ponsol Red Violet 2RNX

There total 2 articles about Ponsol Red Violet 2RNX 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:

13H-Naphtho[2,3-c]acridine-5,8,14-trione (3569-01-5) → 6,10,12-trichloro-13H-naphth[2,3-c]acridine-5,8,14-trione (6373-31-5)

Guidance literature:

With sulfuryl dichloride; iodine; nitrobenzene; at 150 ℃;

Reference yield:

1-anilido-o-carboxy-9,10-anthracene-dione (19795-96-1) → 6,10,12-trichloro-13H-naphth[2,3-c]acridine-5,8,14-trione (6373-31-5)

Guidance literature:

Multi-step reaction with 2 steps

1: thionyl chloride; nitrobenzene / 90 °C / Erhitzen der Reaktionsloesung mit Phosphorylchlorid

2: sulfuryl dichloride; iodine; nitrobenzene / 150 °C

With thionyl chloride; sulfuryl dichloride; iodine; nitrobenzene;

Reference yield:

6,10,12-trichloro-13H-naphth[2,3-c]acridine-5,8,14-trione (6373-31-5) + 3,5-Dichloroaniline (626-43-7) → 10,12-dichloro-6-(3,5-dichloro-anilino)-13H-naphth[2,3-c]acridine-5,8,14-trione (102379-19-1)

Guidance literature:

With naphthalene; sodium acetate;

upstream raw materials:

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

1-anilido-o-carboxy-9,10-anthracene-dione

Downstream raw materials:

10,12-dichloro-6-(3,5-dichloro-anilino)-13H-naphth[2,3-c]acridine-5,8,14-trione