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3,5-Bis-allyloxy-4-bromo-benzoic acid allyl ester

Base Information Edit
  • Chemical Name:3,5-Bis-allyloxy-4-bromo-benzoic acid allyl ester
  • CAS No.:355121-57-2
  • Molecular Formula:C16H17BrO4
  • Molecular Weight:353.213
  • Hs Code.:
  • DSSTox Substance ID:DTXSID001203835
  • Mol file:355121-57-2.mol
3,5-Bis-allyloxy-4-bromo-benzoic acid allyl ester

Synonyms:ICCB1_000151;SCHEMBL6894689;VUCIOGKPUWDSLC-UHFFFAOYSA-N;DTXSID001203835;3,5-Bis-allyloxy-4-bromo-benzoic acid allyl ester;2-Propen-1-yl 4-bromo-3,5-bis(2-propen-1-yloxy)benzoate;355121-57-2

Suppliers and Price of 3,5-Bis-allyloxy-4-bromo-benzoic acid allyl ester
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
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Total 0 raw suppliers
Chemical Property of 3,5-Bis-allyloxy-4-bromo-benzoic acid allyl ester Edit
Chemical Property:
  • XLogP3:4.3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:10
  • Exact Mass:352.03102
  • Heavy Atom Count:21
  • Complexity:347
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C=CCOC1=CC(=CC(=C1Br)OCC=C)C(=O)OCC=C
Technology Process of 3,5-Bis-allyloxy-4-bromo-benzoic acid allyl ester

There total 1 articles about 3,5-Bis-allyloxy-4-bromo-benzoic acid allyl ester 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 potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 15h;
DOI:10.1021/ja016093h
Guidance literature:
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 2h;
DOI:10.1021/ja016093h
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