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1-(Bromomethyl)-3,5-diethoxybenzene

Base Information
  • Chemical Name:1-(Bromomethyl)-3,5-diethoxybenzene
  • CAS No.:238405-74-8
  • Molecular Formula:C11H15BrO2
  • Molecular Weight:259.143
  • Hs Code.:
  • DSSTox Substance ID:DTXSID60593620
  • Wikidata:Q82488133
  • Mol file:238405-74-8.mol
1-(Bromomethyl)-3,5-diethoxybenzene

Synonyms:1-(BROMOMETHYL)-3,5-DIETHOXYBENZENE;238405-74-8;SCHEMBL2935967;DTXSID60593620

Suppliers and Price of 1-(Bromomethyl)-3,5-diethoxybenzene
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
  • Labseeker
  • 1-(bromomethyl)-3,5-diethoxybenzene 95
  • 10g
  • $ 2163.00
  • Labseeker
  • 1-(bromomethyl)-3,5-diethoxybenzene 95
  • 5g
  • $ 1467.00
  • American Custom Chemicals Corporation
  • 1-(BROMOMETHYL)-3,5-DIETHOXYBENZENE 95.00%
  • 5MG
  • $ 500.87
Total 1 raw suppliers
Chemical Property of 1-(Bromomethyl)-3,5-diethoxybenzene
Chemical Property:
  • Boiling Point:322.5±27.0 °C(Predicted) 
  • Density:1.296±0.06 g/cm3(Predicted) 
  • XLogP3:3.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:5
  • Exact Mass:258.02554
  • Heavy Atom Count:14
  • Complexity:138
Purity/Quality:

1-(bromomethyl)-3,5-diethoxybenzene 95 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCOC1=CC(=CC(=C1)CBr)OCC
Technology Process of 1-(Bromomethyl)-3,5-diethoxybenzene

There total 2 articles about 1-(Bromomethyl)-3,5-diethoxybenzene 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 pyridine; phosphorus tribromide; In dichloromethane; at 0 - 20 ℃; for 4h;
DOI:10.1016/j.tet.2016.05.073
Guidance literature:
Multi-step reaction with 2 steps
1: potassium carbonate / acetone / 18 h / Inert atmosphere; Reflux
2: phosphorus tribromide; pyridine / dichloromethane / 4 h / 0 - 20 °C
With pyridine; phosphorus tribromide; potassium carbonate; In dichloromethane; acetone;
DOI:10.1016/j.tet.2016.05.073
Guidance literature:
With N-Bromosuccinimide; In dichloromethane; at 0 ℃; for 1h;
DOI:10.1016/j.tet.2016.05.073
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