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Nefazodone

Base Information
  • Chemical Name:Nefazodone
  • CAS No.:83366-66-9
  • Molecular Formula:C25H32 Cl N5 O2
  • Molecular Weight:470.014
  • Hs Code.:2934.90
  • NSC Number:760344
  • UNII:59H4FCV1TF
  • DSSTox Substance ID:DTXSID2023357
  • Nikkaji Number:J33.097C
  • Wikipedia:Nefazodone
  • Wikidata:Q416632
  • NCI Thesaurus Code:C61859
  • RXCUI:31565
  • Pharos Ligand ID:DKZ9W7B6X819
  • Metabolomics Workbench ID:43371
  • ChEMBL ID:CHEMBL623
  • Mol file:83366-66-9.mol
Nefazodone

Synonyms:Apo-Nefazodone;Dutonin;Lin-Nefazodone;Menfazona;Nefadar;nefazodone;nefazodone hydrochloride;Rulivan;Serzone

Suppliers and Price of Nefazodone
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Medical Isotopes, Inc.
  • NefazodoneHCl
  • 10 mg
  • $ 845.00
  • Crysdot
  • Nefazodone 95+%
  • 1g
  • $ 772.00
  • American Custom Chemicals Corporation
  • NEFAZODONE 95.00%
  • 10G
  • $ 4400.00
  • American Custom Chemicals Corporation
  • NEFAZODONE 95.00%
  • 1G
  • $ 800.00
Total 47 raw suppliers
Chemical Property of Nefazodone
Chemical Property:
  • Appearance/Colour:White to off-white crystalline powder 
  • Melting Point:186 - 188 C 
  • Boiling Point:599.6±60.0 °C(Predicted) 
  • PKA:pKa 6.5 (Uncertain) 
  • PSA:55.53000 
  • Density:1.23±0.1 g/cm3(Predicted) 
  • LogP:3.55480 
  • Storage Temp.:2-8°C 
  • Solubility.:DMSO: ~11 mg/mL at 60 °C 
  • XLogP3:4.3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:10
  • Exact Mass:469.2244530
  • Heavy Atom Count:33
  • Complexity:649
Purity/Quality:

99%, *data from raw suppliers

NefazodoneHCl *data from reagent suppliers

Safty Information:
  • Pictogram(s): UN NO. 
  • Hazard Codes:UN NO. 
  • Safety Statements: 22-24/25 
MSDS Files:

SDS file from LookChem

Useful:
  • Drug Classes:Antidepressant Agents
  • Canonical SMILES:CCC1=NN(C(=O)N1CCOC2=CC=CC=C2)CCCN3CCN(CC3)C4=CC(=CC=C4)Cl
  • Recent ClinicalTrials:Effectiveness of Nefazodone and Bupropion in Treating Marijuana Dependent Individuals
  • Uses A selective serotonin 5-HT2 receptor antagonist. An antidepressant
  • Therapeutic Function Antidepressant
  • Biological Functions Although nefazodone (Serzone) is structurally related to trazodone, it is less sedating. It does not block α1- adrenoreceptors, and its use is not associated with priapism. Nefazodone inhibits the neuronal reuptake of serotonin and blocks 5HT2A receptors. Its short half-life requires dosing twice a day. Nefazodone is not associated with weight gain or sexual dysfunction. It inhibits the cytochrome P450 3A4 isoenzyme that is responsible for 50% of known oxidative metabolism, and therefore, nefazodone can elevate levels of drugs dependent on this pathway for metabolism.
Technology Process of Nefazodone

There total 7 articles about Nefazodone 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:
Guidance literature:
Multi-step reaction with 3 steps
1: toluene / 0.25 h / ice bath
2: 64 percent / KOH / H2O / 0.67 h / 95 - 96 °C
3: 84 percent / 50percent aq. NaOH / propan-2-ol / 7 h / Heating
With potassium hydroxide; sodium hydroxide; In water; isopropyl alcohol; toluene;
DOI:10.1002/jhet.5570220440
Guidance literature:
Multi-step reaction with 4 steps
1: phosgene, imidazole / CH2Cl2 / 2.5 h / 25 °C
2: CH2Cl2 / 16 h / 25 °C
3: 1) 50percent aq. NaOH / 1) water-methylene chloride, 2) xylene, reflux, 2.5 h
4: 84 percent / 50percent aq. NaOH / propan-2-ol / 7 h / Heating
With 1H-imidazole; phosgene; sodium hydroxide; In dichloromethane; isopropyl alcohol;
DOI:10.1002/jhet.5570220440
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