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2-Methoxyidazoxan

Base Information
  • Chemical Name:2-Methoxyidazoxan
  • CAS No.:102575-24-6
  • Molecular Formula:C12H14N2O3
  • Molecular Weight:234.255
  • Hs Code.:
  • UNII:E27LB7P0ET
  • DSSTox Substance ID:DTXSID00907762
  • Nikkaji Number:J246.388A
  • Wikidata:Q27088652
  • Pharos Ligand ID:Y6J52YTFJ9D6
  • Metabolomics Workbench ID:66343
  • ChEMBL ID:CHEMBL10332
  • Mol file:102575-24-6.mol
2-Methoxyidazoxan

Synonyms:2-(2-methoxy-2,3-dihydrobenzo(1,4)dioxin-2-yl)-4,5-dihydro-1H-imidazole;2-methoxyidazoxan;2-methoxyidazoxan hydrochloride;RX 821001;RX 821002;RX-821001;RX-821002;RX821002

Suppliers and Price of 2-Methoxyidazoxan
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
Total 8 raw suppliers
Chemical Property of 2-Methoxyidazoxan
Chemical Property:
  • Vapor Pressure:1.72E-06mmHg at 25°C 
  • Boiling Point:407.9°Cat760mmHg 
  • PKA:9.51±0.40(Predicted) 
  • Flash Point:200.5°C 
  • PSA:52.08000 
  • Density:1.34g/cm3 
  • LogP:0.56660 
  • Storage Temp.:Desiccate at RT 
  • XLogP3:0.5
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:2
  • Exact Mass:234.10044231
  • Heavy Atom Count:17
  • Complexity:321
Purity/Quality:

95% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:COC1(COC2=CC=CC=C2O1)C3=NCCN3
Technology Process of 2-Methoxyidazoxan

There total 4 articles about 2-Methoxyidazoxan 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: N-bromosuccinimide, benzoyl peroxide / CCl4 / 7 h / Heating
2: 80 percent / HCl / diethyl ether / 14 h / 0 °C
3: 26 percent / 24 h / Ambient temperature
With hydrogenchloride; N-Bromosuccinimide; Perbenzoic acid; In tetrachloromethane; diethyl ether;
DOI:10.1021/jm00146a013
Guidance literature:
Multi-step reaction with 2 steps
1: 80 percent / HCl / diethyl ether / 14 h / 0 °C
2: 26 percent / 24 h / Ambient temperature
With hydrogenchloride; In diethyl ether;
DOI:10.1021/jm00146a013
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