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11-Bromo-1-undecanol

Base Information Edit
  • Chemical Name:11-Bromo-1-undecanol
  • CAS No.:1611-56-9
  • Molecular Formula:C11H23BrO
  • Molecular Weight:251.207
  • Hs Code.:29055900
  • European Community (EC) Number:216-554-3
  • NSC Number:4029
  • UNII:P686BA4MWG
  • DSSTox Substance ID:DTXSID00167061
  • Nikkaji Number:J195.234J
  • Wikidata:Q72513674
  • Mol file:1611-56-9.mol
11-Bromo-1-undecanol

Synonyms:11-Bromo-1-undecanol;1611-56-9;11-Bromoundecan-1-ol;11-Bromoundecanol;1-Undecanol, 11-bromo-;1-Bromo-11-hydroxyundecane;11-Bromoundecyl Alcohol;C11H23BrO;MFCD00004752;11-Bromo-1-hydroxyundecane;NSC-4029;EINECS 216-554-3;Undecamethylene bromohydrin;NSC4029;11-bromo-l-undecanol;1-Bromo-11-undecanol;11-bromoundecane-1-ol;omega-Bromoundecyl alcohol;11-Bromoundecanyl alcohol;P686BA4MWG;SCHEMBL290960;C11-H23-Br-O;11-Bromo-1-undecanol, 98%;DTXSID00167061;NSC 4029;AKOS015836181;AM84536;CS-W014623;AS-15413;SY011480;B1477;FT-0607211;A51044;EN300-179511;11-Bromo-1-undecanol, purum, >=99.0% (AT);A810234;J-504143

Suppliers and Price of 11-Bromo-1-undecanol
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
  • TRC
  • 11-?Bromo-?1-?undecanol
  • 50g
  • $ 130.00
  • TRC
  • 11-?Bromo-?1-?undecanol
  • 5g
  • $ 45.00
  • TCI Chemical
  • 11-Bromo-1-undecanol >97.0%(GC)
  • 5g
  • $ 19.00
  • TCI Chemical
  • 11-Bromo-1-undecanol >97.0%(GC)
  • 25g
  • $ 78.00
  • SynQuest Laboratories
  • 11-Bromo-1-undecanol
  • 500 g
  • $ 792.00
  • SynQuest Laboratories
  • 11-Bromo-1-undecanol
  • 25 g
  • $ 135.00
  • SynQuest Laboratories
  • 11-Bromo-1-undecanol
  • 100 g
  • $ 221.00
  • Sigma-Aldrich
  • 11-Bromo-1-undecanol 98%
  • 10g
  • $ 81.80
  • Sigma-Aldrich
  • 11-Bromo-1-undecanol purum, ≥99.0% (AT)
  • 10g
  • $ 61.30
  • Sigma-Aldrich
  • 11-Bromo-1-undecanol purum, ≥99.0% (AT)
  • 50g
  • $ 200.00
Total 87 raw suppliers
Chemical Property of 11-Bromo-1-undecanol Edit
Chemical Property:
  • Appearance/Colour:White to beige crystals or crystalline powder 
  • Vapor Pressure:2.8E-06mmHg at 25°C 
  • Melting Point:46-49 °C(lit.) 
  • Refractive Index:1.476 
  • Boiling Point:349.6 °C at 760 mmHg 
  • PKA:15.20±0.10(Predicted) 
  • Flash Point:122.4 °C 
  • PSA:20.23000 
  • Density:1.137 g/cm3 
  • LogP:3.88450 
  • Storage Temp.:0-10°C 
  • Solubility.:chloroform: soluble50mg/mL, clear to slightly hazy, colorless to 
  • Water Solubility.:Insoluble in water. 
  • XLogP3:5.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:10
  • Exact Mass:250.09323
  • Heavy Atom Count:13
  • Complexity:86.2
Purity/Quality:

99% *data from raw suppliers

11-?Bromo-?1-?undecanol *data from reagent suppliers

Safty Information:
  • Pictogram(s): HarmfulXn 
  • Hazard Codes:Xn 
  • Statements: 20/21/22-36/37/38 
  • Safety Statements: 24/25-36-26 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Chemical Classes:Other Classes -> Halogenated Alcohols
  • Canonical SMILES:C(CCCCCO)CCCCCBr
  • Uses 11-Bromo-1-undecanol was used in the preparation of 11-mercapto-1-undecanol and 1-(2-acryloyloxyundecyl)-3-methylimidazolium bromide. It was used in one-pot synthesis of graft copolymers based on a metathesis skeleton with poly(methyl methacrylate) grafts. 11-Bromo-1-undecanol was used in the preparation of 11-mercapto-1-undecanol and 1-(2-acryloyloxyundecyl)-3-methylimidazolium bromide. It was also used in one-pot synthesis of graft copolymers based on a metathesis skeleton with poly(methyl methacrylate) grafts.
Technology Process of 11-Bromo-1-undecanol

There total 21 articles about 11-Bromo-1-undecanol 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 hydrogenchloride; In tetrahydrofuran; diethylene glycol dimethyl ether; water;
Guidance literature:
With hydrogenchloride; aluminium trichloride; In diethylene glycol dimethyl ether; water;
Guidance literature:
With lithium aluminium tetrahydride; In diethyl ether; at 0 ℃; for 0.666667h;
DOI:10.1246/bcsj.67.455
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