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B-IODO-9-BBN

Base Information
  • Chemical Name:B-IODO-9-BBN
  • CAS No.:70145-42-5
  • Molecular Formula:C8H14BI
  • Molecular Weight:247.915
  • Hs Code.:
  • Mol file:70145-42-5.mol
B-IODO-9-BBN

Synonyms:9-IODO-9-BORABICYCLO[3.3.1]NONANE;B-IODO-9-BBN;B-IODO-9-BBN, 1.0M SOLUTION IN HEXANES;B-IODO-9-BBN 97%;9-iodo-9-borabicyclo[3.3.1]nonane solution;b-iodo-9-bbn solution

Suppliers and Price of B-IODO-9-BBN
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
  • Sigma-Aldrich
  • B-Iodo-9-BBN solution 1.0 M in hexanes
  • 25ml
  • $ 158.00
Total 24 raw suppliers
Chemical Property of B-IODO-9-BBN
Chemical Property:
  • Vapor Pressure:0.0409mmHg at 25°C 
  • Refractive Index:1.528 
  • Boiling Point:55 °C/0.2 mmHg(lit.) 
  • Flash Point:−9 °F  
  • PSA:0.00000 
  • Density:0.816 g/mL at 25 °C  
  • LogP:3.52110 
  • Storage Temp.:Room Temperature, under inert atmosphere 
  • Solubility.:solution in hexanes, not soluble in aqueous media 
Purity/Quality:

98%,99%, *data from raw suppliers

B-Iodo-9-BBN solution 1.0 M in hexanes *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:F,C,N,Xn 
  • Statements: 11-34-17-67-65-62-51/53-48/20-38 
  • Safety Statements: 16-26-27-36/37/39-45-62-61-36/37 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses B-?IODO-?9-?BBN is a coupling reagent used in the synthesis of cannabilactones, which act as a novel class of selective CB2 agonists.
Technology Process of B-IODO-9-BBN

There total 5 articles about B-IODO-9-BBN 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 boron triiodide; In pentane; Heating;
DOI:10.1016/S0022-328X(00)83211-8
Guidance literature:
Multi-step reaction with 4 steps
1: CH2Cl2 / Ambient temperature
2: BBr3 / pentane / Heating
3: CH2Cl2 / Ambient temperature
4: BI3 / pentane / Heating
With boron triiodide; boron tribromide; In dichloromethane; pentane;
DOI:10.1016/S0022-328X(00)83211-8
Guidance literature:
Multi-step reaction with 4 steps
1: CH2Cl2 / Ambient temperature
2: BCl3 / pentane
3: CH2Cl2 / Ambient temperature
4: BI3 / pentane / Heating
With boron triiodide; boron trichloride; In dichloromethane; pentane;
DOI:10.1016/S0022-328X(00)83211-8
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