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1-Bromotetracosane

Base Information Edit
  • Chemical Name:1-Bromotetracosane
  • CAS No.:6946-24-3
  • Molecular Formula:C24H49Br
  • Molecular Weight:417.5499
  • Hs Code.:
  • NSC Number:56731
  • DSSTox Substance ID:DTXSID00288588
  • Nikkaji Number:J2.309.053H
  • Wikidata:Q82025667
  • Mol file:6946-24-3.mol
1-Bromotetracosane

Synonyms:1-Bromotetracosane;Tetracosane, 1-bromo-;6946-24-3;NSC 56731;NSC56731;1-tetracosyl bromide;SCHEMBL3065700;DTXSID00288588;NSC-56731;AKOS024429733;FT-0700922

Suppliers and Price of 1-Bromotetracosane
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
  • Packaging
  • price
Total 4 raw suppliers
Chemical Property of 1-Bromotetracosane Edit
Chemical Property:
  • Vapor Pressure:5.88E-07mmHg at 25°C 
  • Melting Point:50.7°C 
  • Refractive Index:1.4862 (estimate) 
  • Boiling Point:422.5°Cat760mmHg 
  • Flash Point:176.8°C 
  • PSA:0.00000 
  • Density:0.953g/cm3 
  • LogP:9.98340 
  • XLogP3:13.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:22
  • Exact Mass:416.30176
  • Heavy Atom Count:25
  • Complexity:214
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCCCCCCCCCCCCCCCCCCCBr
Technology Process of 1-Bromotetracosane

There total 8 articles about 1-Bromotetracosane 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 N-Bromosuccinimide; triphenylphosphine; In dichloromethane; at 20 ℃; for 5h;
DOI:10.1016/j.tet.2005.09.056
Guidance literature:
Multi-step reaction with 5 steps
1: 78 percent / n-BuLi / hexamethylphosphoric acid triamide
2: ethylenediamine, NaH / 45 - 55 °C
3: 1.) n-BuLi / 1.) HMPA. 2.) HMPA
4: H2 / Pd/C / ethanol
5: 48percent aq. HBr, conc. H2SO4 / 90 - 110 °C
With n-butyllithium; sulfuric acid; hydrogen bromide; hydrogen; sodium hydride; ethylenediamine; palladium on activated charcoal; In N,N,N,N,N,N-hexamethylphosphoric triamide; ethanol;
DOI:10.1021/ja00062a086
Guidance literature:
Multi-step reaction with 3 steps
1: 1.) n-BuLi / 1.) HMPA. 2.) HMPA
2: H2 / Pd/C / ethanol
3: 48percent aq. HBr, conc. H2SO4 / 90 - 110 °C
With n-butyllithium; sulfuric acid; hydrogen bromide; hydrogen; palladium on activated charcoal; In ethanol;
DOI:10.1021/ja00062a086
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