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1-Bromo-2-[4-(2-bromophenoxy)butoxy]benzene

Base Information
  • Chemical Name:1-Bromo-2-[4-(2-bromophenoxy)butoxy]benzene
  • CAS No.:61739-61-5
  • Molecular Formula:C16H16Br2O2
  • Molecular Weight:400.11
  • Hs Code.:
  • DSSTox Substance ID:DTXSID30367916
  • Wikidata:Q82154097
1-Bromo-2-[4-(2-bromophenoxy)butoxy]benzene

Synonyms:1-bromo-2-[4-(2-bromophenoxy)butoxy]benzene;61739-61-5;Benzene, 1,1'-[1,4-butanediylbis(oxy)]bis[2-bromo-;SCHEMBL2344935;DTXSID30367916

Suppliers and Price of 1-Bromo-2-[4-(2-bromophenoxy)butoxy]benzene
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Chemical Property of 1-Bromo-2-[4-(2-bromophenoxy)butoxy]benzene
Chemical Property:
  • XLogP3:5.7
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:7
  • Exact Mass:399.94966
  • Heavy Atom Count:20
  • Complexity:237
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C(=C1)OCCCCOC2=CC=CC=C2Br)Br
Technology Process of 1-Bromo-2-[4-(2-bromophenoxy)butoxy]benzene

There total 1 articles about 1-Bromo-2-[4-(2-bromophenoxy)butoxy]benzene 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:
2-hydroxybromobenzene; With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h; Inert atmosphere;
1,4-dibromo-butane; In N,N-dimethyl-formamide; at 20 ℃; for 16h; Inert atmosphere;
DOI:10.1002/ejic.201900716
Guidance literature:
1-bromo-2-[4-(2-bromophenoxy)butoxy]benzene; With n-butyllithium; In diethyl ether; hexane; at -78 ℃;
Triisopropyl borate; In diethyl ether; hexane; at -78 - 20 ℃; for 16h;
With water; In diethyl ether; hexane; Acidic conditions;
DOI:10.1002/ejic.201900716
Guidance literature:
With n-butyllithium; In tetrahydrofuran; hexane; benzene; stirring of ligand precursor (in THF) with BuLi (in hexane) for 15 min, addn. of suspn. of Ni-complex (in C6H6), stirring for 20 h; evapn., extn. into hot heptane, volume reduction (crystn.); elem. anal.;
DOI:10.1039/DT9760002053
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