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Dichloro(isopropyl)borane

Base Information Edit
  • Chemical Name:Dichloro(isopropyl)borane
  • CAS No.:7680-99-1
  • Molecular Formula:C3H7BCl2
  • Molecular Weight:124.806
  • Hs Code.:
  • DSSTox Substance ID:DTXSID901307769
  • Nikkaji Number:J539.515A
  • Mol file:7680-99-1.mol
Dichloro(isopropyl)borane

Synonyms:dichloro(isopropyl)borane;dichloro(2-propyl)borane;dichloro-propan-2-ylborane;Dichloro(1-methylethyl)borane;SCHEMBL3886316;LMLFCQYNWULLLD-UHFFFAOYSA-N;DTXSID901307769;7680-99-1

Suppliers and Price of Dichloro(isopropyl)borane
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
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Chemical Property of Dichloro(isopropyl)borane Edit
Chemical Property:
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:0
  • Exact Mass:124.0017858
  • Heavy Atom Count:6
  • Complexity:35.8
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:B(C(C)C)(Cl)Cl
Technology Process of Dichloro(isopropyl)borane

There total 3 articles about Dichloro(isopropyl)borane 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:
byproducts: boron hydride, benzene, C3H8; High Pressure; under N2; diborane and trihalogen-borane was added to cumene at -130°C, then in a closed autoclave the mixture was heated to 130°C for 90 min; at -195.8°C H2 was removed, at room temp. the residue of trihalogen-borane and diborane were removed, unseparable isomers; elem. anal.;
Guidance literature:
With boron trichloride;
DOI:10.1021/ja01576a027
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