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desmethylazelastine

Base Information Edit
  • Chemical Name:desmethylazelastine
  • CAS No.:47491-38-3
  • Molecular Formula:C21H22 Cl N3 O
  • Molecular Weight:367.878
  • Hs Code.:
  • Mol file:47491-38-3.mol
desmethylazelastine

Synonyms:Demethylazelastine;Desmethylazelastine

Suppliers and Price of desmethylazelastine
Supply Marketing:Edit
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
  • TRC
  • N-DesmethylAzelastine
  • 100mg
  • $ 1455.00
  • TRC
  • N-DesmethylAzelastine
  • 10mg
  • $ 185.00
  • Medical Isotopes, Inc.
  • N-DesmethylAzelastine
  • 12.5 mg
  • $ 3250.00
  • Biosynth Carbosynth
  • N-Desmethyl azelastine
  • 25 mg
  • $ 3071.50
  • Biosynth Carbosynth
  • N-Desmethyl azelastine
  • 10 mg
  • $ 1689.30
  • Biosynth Carbosynth
  • N-Desmethyl azelastine
  • 1 mg
  • $ 281.10
  • Biosynth Carbosynth
  • N-Desmethyl azelastine
  • 5 mg
  • $ 929.10
  • Biosynth Carbosynth
  • N-Desmethyl azelastine
  • 2 mg
  • $ 511.00
  • American Custom Chemicals Corporation
  • DESMETHYLAZELASTINE 95.00%
  • 5MG
  • $ 498.07
Total 9 raw suppliers
Chemical Property of desmethylazelastine Edit
Chemical Property:
  • Vapor Pressure:6.76E-12mmHg at 25°C 
  • Boiling Point:544.1°Cat760mmHg 
  • Flash Point:282.8°C 
  • PSA:46.92000 
  • Density:1.29g/cm3 
  • LogP:4.28410 
  • Storage Temp.:Refrigerator 
  • Solubility.:Chloroform (Slightly), Methanol (Slightly) 
Purity/Quality:

99% *data from raw suppliers

N-DesmethylAzelastine *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses The main phase I metabolites of Azelastine. The main phase I metabolites of Azelastine
Technology Process of desmethylazelastine

There total 6 articles about desmethylazelastine 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:
1,1-dimethylethyl 4-[4-[(4-chlorophenyl)methyl]-1-oxo-2(1H)-phthalazinyl]hexahydro-1H-azepine-1-carboxylate; With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 1.5h;
With ammonia; In methanol;
Guidance literature:
Multi-step reaction with 2 steps
1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 3.58 h / -20 - 20 °C
2: hydrogenchloride / 1,4-dioxane / 1.5 h / 20 °C
With hydrogenchloride; di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; 1,4-dioxane;
Guidance literature:
Multi-step reaction with 4 steps
1.1: sodium acetate / 1-methyl-pyrrolidin-2-one / 48 h / 200 °C
2.1: hydrazine / ethanol / 15 h / 85 °C
2.2: 2 h / 2 °C
3.1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 3.58 h / -20 - 20 °C
4.1: hydrogenchloride / 1,4-dioxane / 1.5 h / 20 °C
With hydrogenchloride; di-isopropyl azodicarboxylate; sodium acetate; triphenylphosphine; hydrazine; In tetrahydrofuran; 1,4-dioxane; 1-methyl-pyrrolidin-2-one; ethanol;
Refernces Edit
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