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CID 6327220

Base Information Edit
  • Chemical Name:CID 6327220
  • CAS No.:13709-65-4
  • Molecular Formula:BBr2 H
  • Molecular Weight:171.627
  • Hs Code.:
  • DSSTox Substance ID:DTXSID90929711
  • Wikidata:Q82904776
  • Mol file:13709-65-4.mol
CID 6327220

Synonyms:BBr2;BHBr2;DTXSID90929711

Suppliers and Price of CID 6327220
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
Total 1 raw suppliers
Chemical Property of CID 6327220 Edit
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:0.00000 
  • Density:g/cm3 
  • LogP:1.04270 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:0
  • Exact Mass:170.84393
  • Heavy Atom Count:3
  • Complexity:2.8
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:[B](Br)Br
Technology Process of CID 6327220

There total 18 articles about CID 6327220 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 neat (no solvent); Teflon-valve-equipped standard vacuum line or a nitrogen-filled glovebox;3 aliquots of BBr3 added to BCl2B5H8, stirred, while reactor was held at -78 ° C, volatile material removed at -78 ° C, reactor warmed to -10 ° C; fractionation,identification by boron NMR and mass spectroscopy; small amts. of B2H6, BCl2H, BBr2H, and mixed boron trihalides;
Guidance literature:
In neat (no solvent); Teflon-valve-equipped standard vacuum line or a nitrogen-filled glovebox;excess B5H9;pentaborane, B2Br4 separately condensed in the reactor, after 20 min at room temp., vessel cooled to -10 ° C,; over course of the following 10 h,all volatile material removed,reactor warmed to room temp.,all volatile material at room temp. were removed,BBr2B5H8 extd. with CH2Cl2, yield:80% on basis of amt. of B2Br4 employed, 86% on basis of unrecovered B5H9;
Guidance literature:
With Na or Al; 160-200 bar; 150°C; IR spectrum of react. mixt.;
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