Dibenzepin

Base Information

• Chemical Name: Dibenzepin
• CAS No.: 4498-32-2
• Molecular Formula: C18H21 N3 O
• Molecular Weight: 295.384
• Hs Code.: 2933990090
• UNII: 510SJZ1Y6L
• DSSTox Substance ID: DTXSID7022916
• Nikkaji Number: J8.740H
• Wikipedia: Dibenzepin
• Wikidata: Q412107
• NCI Thesaurus Code: C166799
• Pharos Ligand ID: NGL1M94WKSH1
• Metabolomics Workbench ID: 144286
• ChEMBL ID: CHEMBL1442422
• Mol file: 4498-32-2.mol

Synonyms:dibenzepin;dibenzepin hydrochloride;Noveril

Chemical Property of Dibenzepin

Chemical Property:

• Vapor Pressure: 2.39E-08mmHg at 25°C
• Melting Point: 116-117°C
• Refractive Index: 1.5855 (estimate)
• Boiling Point: 451.7°Cat760mmHg
• PKA: 8.25(at 25℃)
• Flash Point: 194.9°C
• PSA: 30.17000
• Density: 1.134g/cm³
• LogP: 2.61700
• Storage Temp.: Refrigerator
• XLogP3: 2.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 295.168462302
• Heavy Atom Count: 22
• Complexity: 398

Purity/Quality:

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

Dibenzepin ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CN1C2=CC=CC=C2C(=O)N(C3=CC=CC=C31)CCN(C)C
• Uses: Antidepressant
• Therapeutic Function: Psychostimulant

Technology Process of Dibenzepin

There total 1 articles about Dibenzepin 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:

→ dibenzepin (4498-32-2)

Guidance literature:

Aus der Aminosaeure durch Cyclisierung;

Reference yield:

dibenzepin (4498-32-2) → N-Methyl-2-<β-methylamino-aethyl>-diphenylamin

Guidance literature:

Multistep reaction; (i) ClCO₂Et, (ii) (acid hydrolysis);

DOI:10.1002/hlca.19650480721