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Dilithium;trichlorolanthanum;dichloride

Base Information
  • Chemical Name:Dilithium;trichlorolanthanum;dichloride
  • CAS No.:405204-22-0
  • Molecular Formula:Cl5LaLi2
  • Molecular Weight:323.1
  • Hs Code.:
  • DSSTox Substance ID:DTXSID80746237
Dilithium;trichlorolanthanum;dichloride

Synonyms:405204-22-0;dilithium;trichlorolanthanum;dichloride;LaCl3.2LiCl;DTXSID80746237;Lithium chloride--trichlorolanthanum (2/2/1)

Suppliers and Price of Dilithium;trichlorolanthanum;dichloride
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
  • Lanthanum(III) chloride bis(lithium chloride) complex solution 0.6 M in THF
  • 4x25ml
  • $ 182.00
  • Sigma-Aldrich
  • Lanthanum(III) chloride bis(lithium chloride) complex solution 0.6 M in THF
  • 100ml
  • $ 137.00
  • Sigma-Aldrich
  • Lanthanum(III) chloride bis(lithium chloride) complex solution 0.6 M in THF
  • 25ml
  • $ 58.90
  • American Custom Chemicals Corporation
  • LANTHANUM TRICHLORIDE LITHIUM CHLORIDE COMPLEX 95.00%
  • 5MG
  • $ 505.69
Total 45 raw suppliers
Chemical Property of Dilithium;trichlorolanthanum;dichloride
Chemical Property:
  • Flash Point:17℃ 
  • PSA:0.00000 
  • Density:1.05 g/mL at 25 °C 
  • LogP:-14.98000 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:0
  • Exact Mass:329.779683
  • Heavy Atom Count:8
  • Complexity:8
Purity/Quality:

98%,99%, *data from raw suppliers

Lanthanum(III) chloride bis(lithium chloride) complex solution 0.6 M in THF *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:F,Xn 
  • Statements: 11-19-36/37/38-40 
  • Safety Statements: 16-26-36/37 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:[Li+].[Li+].[Cl-].[Cl-].Cl[La](Cl)Cl
  • Uses Selective 1,2-Additions with LaCl3?2LiClMediates Grignard additionsReagent for metal exchange reactionsPromoter for the addition of organometallic compounds to sterically hindered, enolizable or α,β-unsaturated ketones or imines
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