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Pentaborane(9),1-bromo- (6CI,7CI,8CI,9CI)

Base Information
  • Chemical Name:Pentaborane(9),1-bromo- (6CI,7CI,8CI,9CI)
  • CAS No.:23753-67-5
  • Molecular Formula:B5Br H8
  • Molecular Weight:142.023
  • Hs Code.:
Pentaborane(9),1-bromo- (6CI,7CI,8CI,9CI)

Synonyms:1-Bromooctahydropentaborane;1-Bromopentaborane(9)

Suppliers and Price of Pentaborane(9),1-bromo- (6CI,7CI,8CI,9CI)
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 3 raw suppliers
Chemical Property of Pentaborane(9),1-bromo- (6CI,7CI,8CI,9CI)
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Safety Statements:Ignites spontaneously in air. Explosive reaction with hexamine a"> −. See also BORANES and BORON COMPOUNDS." target="_blank">Ignites spontaneously in air. Explosive reaction with hexamine a 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of Pentaborane(9),1-bromo- (6CI,7CI,8CI,9CI)

There total 3 articles about Pentaborane(9),1-bromo- (6CI,7CI,8CI,9CI) 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 bromine; excess of Br2;;
Guidance literature:
With hydrogen bromide; at elevated temp.;;
Guidance literature:
With HBr; In dichloromethane; byproducts: H2; HBr condensing onto ammonium borate in CH2Cl2 at -196°C, warmingto -78°C for 1 h, then stirring at room temp.for several minutes, BBr3 and CH2Cl2 condensing at -196°C, stirring at -78°C for 12 h, fractionating; identified by IR and NMR spectra;
DOI:10.1021/ic00135a048
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