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11-BroMo-1-undecanethiol

Base Information
  • Chemical Name:11-BroMo-1-undecanethiol
  • CAS No.:116129-34-1
  • Molecular Formula:C11H23BrS
  • Molecular Weight:267.26900
  • Hs Code.:2930909090
  • Mol file:116129-34-1.mol
11-BroMo-1-undecanethiol

Synonyms:1-Undecanethiol,11-bromo;11-Bromo-1-undecanethiol;11-bromoundecanethiol;

Suppliers and Price of 11-BroMo-1-undecanethiol
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
  • Sigma-Aldrich
  • 11-Bromo-1-undecanethiol 99%
  • 250mg
  • $ 279.00
  • American Custom Chemicals Corporation
  • 11-BROMO-1-UNDECANETHIOL 95.00%
  • 250MG
  • $ 759.18
Total 7 raw suppliers
Chemical Property of 11-BroMo-1-undecanethiol
Chemical Property:
  • Refractive Index:n20/D1.501 
  • PSA:38.80000 
  • Density:1.128 g/mL at 25 °C 
  • LogP:4.82200 
  • Storage Temp.:?20°C 
Purity/Quality:

98%,99%, *data from raw suppliers

11-Bromo-1-undecanethiol 99% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36/37 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses BrUDT forms a protective SAM on gold nanoparticles, which can be potentially used in biomedical applications for the fabrication of in vivo sensors. It can also be mixed with dodecanethiol, which can be coated on gold nanoparticles for the synthesis of gasotransmitters.
Technology Process of 11-BroMo-1-undecanethiol

There total 4 articles about 11-BroMo-1-undecanethiol 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 acetyl chloride; In methanol; at 0 - 20 ℃; for 3h; Inert atmosphere;
DOI:10.1002/pola.24782
Guidance literature:
With tetraphosphorus decasulfide; In toluene; for 3h; Reflux;
DOI:10.1055/s-0036-1589026
Guidance literature:
Multi-step reaction with 2 steps
1: AiBN / toluene / 2 h / Heating
2: HCl; acetyl chloride; methanol / 6 h / 20 °C
With hydrogenchloride; methanol; 2,2'-azobis(isobutyronitrile); acetyl chloride; In toluene;
DOI:10.1021/ja052027u
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