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1,4-Bis(2-bromoethyl)-2,5-dimethoxybenzene

Base Information
  • Chemical Name:1,4-Bis(2-bromoethyl)-2,5-dimethoxybenzene
  • CAS No.:64425-63-4
  • Molecular Formula:C12H16Br2O2
  • Molecular Weight:352.066
  • Hs Code.:
  • DSSTox Substance ID:DTXSID50493589
  • Wikidata:Q82340362
1,4-Bis(2-bromoethyl)-2,5-dimethoxybenzene

Synonyms:1,4-Bis(2-bromoethyl)-2,5-dimethoxybenzene;64425-63-4;DTXSID50493589

Suppliers and Price of 1,4-Bis(2-bromoethyl)-2,5-dimethoxybenzene
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
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Total 0 raw suppliers
Chemical Property of 1,4-Bis(2-bromoethyl)-2,5-dimethoxybenzene
Chemical Property:
  • Melting Point:122-123 °C 
  • Boiling Point:368.8±37.0 °C(Predicted) 
  • PSA:18.46000 
  • Density:1.534±0.06 g/cm3(Predicted) 
  • LogP:3.57860 
  • XLogP3:4.3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:6
  • Exact Mass:351.94966
  • Heavy Atom Count:16
  • Complexity:170
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:COC1=CC(=C(C=C1CCBr)OC)CCBr
Technology Process of 1,4-Bis(2-bromoethyl)-2,5-dimethoxybenzene

There total 8 articles about 1,4-Bis(2-bromoethyl)-2,5-dimethoxybenzene 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:
With carbon tetrabromide; triphenylphosphine; In dichloromethane; at 0 - 20 ℃; for 4h;
DOI:10.1016/j.ejmech.2017.09.021
Guidance literature:
Multi-step reaction with 2 steps
1: LiAlH4 / tetrahydrofuran
2: PBr3 / benzene
With lithium aluminium tetrahydride; phosphorus tribromide; In tetrahydrofuran; benzene;
Guidance literature:
Multi-step reaction with 6 steps
1: ammonium hydroxide / water; ethanol
2: hydrogenchloride / water / 20 h / Reflux
3: sodium hydroxide / 50 °C
4: thionyl chloride / 0 - 20 °C
5: lithium aluminium tetrahydride / tetrahydrofuran / 1 h
6: carbon tetrabromide; triphenylphosphine / dichloromethane / 4 h / 0 - 20 °C
With hydrogenchloride; ammonium hydroxide; lithium aluminium tetrahydride; thionyl chloride; carbon tetrabromide; triphenylphosphine; sodium hydroxide; In tetrahydrofuran; ethanol; dichloromethane; water;
DOI:10.1016/j.ejmech.2017.09.021
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