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Boronic acid, bis(1,1-diethylpropyl) ester

Base Information
  • Chemical Name:Boronic acid, bis(1,1-diethylpropyl) ester
  • CAS No.:144782-40-1
  • Molecular Formula:C14H31BO2
  • Molecular Weight:242.21
  • Hs Code.:
  • DSSTox Substance ID:DTXSID70478535
  • Wikidata:Q82311996
  • Mol file:144782-40-1.mol
Boronic acid, bis(1,1-diethylpropyl) ester

Synonyms:Boronic acid, bis(1,1-diethylpropyl) ester;144782-40-1;DTXSID70478535

Suppliers and Price of Boronic acid, bis(1,1-diethylpropyl) ester
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 2 raw suppliers
Chemical Property of Boronic acid, bis(1,1-diethylpropyl) ester
Chemical Property:
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:10
  • Exact Mass:241.2338854
  • Heavy Atom Count:17
  • Complexity:150
Purity/Quality:

99.90% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:[B](OC(CC)(CC)CC)OC(CC)(CC)CC
Technology Process of Boronic acid, bis(1,1-diethylpropyl) ester

There total 2 articles about Boronic acid, bis(1,1-diethylpropyl) ester 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 tetrahydrofuran; byproducts: H2; under inert atm.; excess of alcohol in THF added dropwise at room temp. to stirred soln. of tetrahydroborate complex in THF (accompanied by vigorous gas evolution); stirring was continued for 1 h; mixt. allowed to stand for the reaction to be completed; within 5 ds ppt. sepd. by filtration (identified as NaBH4 by X-ray diffraction and IR spectroscopy); filtrate was distd. (vac., 0.1 mmHg) at room temp. to remove solvent and at 50°C; residue pumped out at 100-115°C; volatile collected ...;
Guidance literature:
In tetrahydrofuran; byproducts: H2; under inert atm.; excess of alcohol in THF added dropwise at room temp. to stirred soln. of tetrahydroborate complex in THF (accompanied by vigorous gas evolution); stirring was continued for 1 h; mixt. allowed to stand for the reaction to be completed; within 5 ds ppt. sepd. by filtration (identified as NaBH4 by X-ray diffraction and IR spectroscopy); filtrate was distd. (vac., 0.1 mmHg) at room temp. to remove solvent and at 50°C; residue pumped out at 100-115°C; volatile collected ...;
upstream raw materials:

3-ethylpentan-3-ol

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