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Tris(2-methylprop-2-en-1-yl) borate

Base Information
  • Chemical Name:Tris(2-methylprop-2-en-1-yl) borate
  • CAS No.:78538-54-2
  • Molecular Formula:C12H21BO3
  • Molecular Weight:224.108
  • Hs Code.:
  • NSC Number:92798
  • DSSTox Substance ID:DTXSID50293889
  • Wikidata:Q82032886
Tris(2-methylprop-2-en-1-yl) borate

Synonyms:78538-54-2;tris(2-methylprop-2-en-1-yl) borate;NSC92798;DTXSID50293889;tris(2-methyl-2-propenyl) borate;NSC-92798;AKOS024332494

Suppliers and Price of Tris(2-methylprop-2-en-1-yl) borate
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
Total 7 raw suppliers
Chemical Property of Tris(2-methylprop-2-en-1-yl) borate
Chemical Property:
  • Vapor Pressure:0.114mmHg at 25°C 
  • Boiling Point:227.9°Cat760mmHg 
  • Flash Point:59.8°C 
  • Density:0.888g/cm3 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:9
  • Exact Mass:224.1583747
  • Heavy Atom Count:16
  • Complexity:218
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:B(OCC(=C)C)(OCC(=C)C)OCC(=C)C
Technology Process of Tris(2-methylprop-2-en-1-yl) borate

There total 4 articles about Tris(2-methylprop-2-en-1-yl) borate 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:
In benzene; byproducts: ethanol; exclusion of moisture; a mixt. of metal alkoxide and methallyl alcohol in dry benzene was refluxed with fractional sepn. of alcohol/benzene azeotrope;; removal of solvent under reduced pressure; distn. (vac.); elem. anal.;;
Guidance literature:
In benzene; exclusion of moisture; a mixt. of B2O3 and HOCH2C(CH3)CH2 in dry benzene was refluxed with fractional sepn. of the formed H2O;; removal of solvent under reduced pressure; distn. (vac.); elem. anal.;;
Guidance literature:
In neat (no solvent); exclusion of moisture; disproportionation by heating of alkenoxy boroxine to 100-135°C/1.0 mmHg (a much higher temp. then b.p. of corresponding orthoborate);
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