Dibenz[c,h]acridine

Base Information

• Chemical Name: Dibenz[c,h]acridine
• CAS No.: 224-53-3
• Molecular Formula: C21H13 N
• Molecular Weight: 279.35
• Hs Code.: 2933990090
• European Community (EC) Number: 681-926-8
• UNII: 5L5784WI2U
• DSSTox Substance ID: DTXSID30176929
• Nikkaji Number: J2.976I
• Wikidata: Q27262515
• Mol file: 224-53-3.mol

Synonyms:dibenz(c,h)acridine

Chemical Property of Dibenz[c,h]acridine

Chemical Property:

• Appearance/Colour: Powder.
• Vapor Pressure: 6.07E-11mmHg at 25°C
• Melting Point: 191ºC
• Refractive Index: 1.8240 (estimate)
• Boiling Point: 534 °C at 760 mmHg
• PKA: 4.25±0.30(Predicted)
• Flash Point: 240.3 °C
• PSA: 12.89000
• Density: 1.274 g/cm³
• LogP: 5.69440
• Storage Temp.: 2-8°C
• Water Solubility.: 19.55ug/L(22 oC)
• XLogP3: 6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 279.104799419
• Heavy Atom Count: 22
• Complexity: 369

Purity/Quality:

98%Min ^*data from raw suppliers

Dibenz[c,h]acridine BCR ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Other Classes -> Polycyclic Aromatic Hydrocarbons
• Canonical SMILES: C1=CC=C2C(=C1)C=CC3=C2N=C4C(=C3)C=CC5=CC=CC=C54

Technology Process of Dibenz[c,h]acridine

There total 24 articles about Dibenz[c,h]acridine 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: 94.0%

5,6-dihydro-dibenz[c,h]acridine → dibenz[c,h]acridine (224-53-3)

Guidance literature:

palladium on activated charcoal; In various solvent(s); Heating;

DOI:10.1246/cl.1992.1739

Reference yield: 75.0%

5,6,8,9-tetrahydrodibenzacridine (6581-76-6) → dibenz[c,h]acridine (224-53-3)

Guidance literature:

With 2,3-dicyano-5,6-dichloro-p-benzoquinone; In 1,4-dioxane; at 80 ℃; for 72h; Inert atmosphere;

DOI:10.1021/acs.organomet.0c00015

Reference yield: 11.0%

(S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1R,2R)-2-bromo-1,2,3,4-tetrahydro-dibenzo[c,h]acridin-1-yl ester (93716-18-8,93781-01-2) → dibenz[c,h]acridine (224-53-3) + (+)-(1R,2S)-1,2-epoxy-1,2,3,4-tetrahydrodibenzacridine (93781-05-6)

Guidance literature:

With sodium methylate; In tetrahydrofuran; at 0 - 5 ℃; for 312h;

DOI:10.1021/jo00201a019

upstream raw materials:

dibenzoacridine

diiodomethane

1-amino-naphthalene

dichloromethane

Downstream raw materials:

cis-5,6-dihydroxy-5,6-dihydrodibenzacridine

trans-5,6-dihydroxy-5,6-dihydrodibenzacridine

Dibenz-acridin-5,6-oxid-N-oxid

4b,5a-dihydrodibenzoxirenoacridine

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