Benzamide, N-(5-chloro-4-methoxyanthraquinonyl)-

Base Information

• Chemical Name: Benzamide, N-(5-chloro-4-methoxyanthraquinonyl)-
• CAS No.: 116-80-3
• Molecular Formula: C₂₂H₁₄ClNO₄
• Molecular Weight: 391.81
• Hs Code.: 2924299090
• DSSTox Substance ID: DTXSID80151261
• Nikkaji Number: J54.762J
• Wikidata: Q83017687
• Mol file: 116-80-3.mol

Synonyms:116-80-3;BENZAMIDE, N-(5-CHLORO-4-METHOXYANTHRAQUINONYL)-;n-(5-chloro-4-methoxy-9,10-dioxo-9,10-dihydroanthracen-1-yl)benzamide;BRN 2783838;N-(5-Chloro-4-methoxyanthraquinonyl)benzamide;N-(5-chloro-4-methoxy-9,10-dioxoanthracen-1-yl)benzamide;1-Benzoylamino-4-methoxy-5-chloranthrachinon [Czech];1-Benzoylamino-5-chlor-4-methoxyanthrachinon [Czech];1-Benzoylamino-4-methoxy-5-chloranthrachinon;1-Benzoylamino-5-chlor-4-methoxyanthrachinon;2-14-00-00172 (Beilstein Handbook Reference);C22H14ClNO4;C22-H14-Cl-N-O4;DTXSID80151261;LS-26121;N-(5-Chloro-9,10-dihydro-4-methoxy-9,10-dioxoanthracen-1-yl)benzamide

Chemical Property of Benzamide, N-(5-chloro-4-methoxyanthraquinonyl)-

Chemical Property:

• Vapor Pressure: 1.47E-11mmHg at 25°C
• Refractive Index: 1.6910 (estimate)
• Boiling Point: 535.9°Cat760mmHg
• Flash Point: 277.9°C
• PSA: 72.47000
• Density: 1.43g/cm³
• LogP: 4.44930
• XLogP3: 4.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 391.0611356
• Heavy Atom Count: 28
• Complexity: 632

Purity/Quality:

98%,99%, ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=C2C(=C(C=C1)NC(=O)C3=CC=CC=C3)C(=O)C4=C(C2=O)C(=CC=C4)Cl

Technology Process of Benzamide, N-(5-chloro-4-methoxyanthraquinonyl)-

There total 2 articles about Benzamide, N-(5-chloro-4-methoxyanthraquinonyl)- 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-benzoylamino-5-chloro-4-hydroxy-anthraquinone (134217-43-9) → 1-Benzoylamino-5-chlor-4-methoxy-anthrachinon (116-80-3)

Guidance literature:

With magnesium oxide; nitrobenzene; beim Methylieren;

Reference yield:

1-amino-5-chloro-4-methoxy-anthraquinone (873981-77-2) → 1-Benzoylamino-5-chlor-4-methoxy-anthrachinon (116-80-3)

Guidance literature:

durch Benzoylieren;

Reference yield:

1-Benzoylamino-5-chlor-4-methoxy-anthrachinon (116-80-3) + toluene-4-sulfonamide (70-55-3) → 5-amino-1-benzoylamino-4-methoxy-anthraquinone

Guidance literature:

With copper diacetate; potassium carbonate; nitrobenzene; Behandeln des Reaktionsprodukts mit Schwefelsaeure;

upstream raw materials:

1-amino-5-chloro-4-methoxy-anthraquinone

1-benzoylamino-5-chloro-4-hydroxy-anthraquinone

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