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1,2-Bis(dimethylarsino)benzene

Base Information
  • Chemical Name:1,2-Bis(dimethylarsino)benzene
  • CAS No.:13246-32-7
  • Molecular Formula:C10H16 As2
  • Molecular Weight:286.08
  • Hs Code.:2931900090
  • European Community (EC) Number:236-227-9
  • NSC Number:89290
  • UNII:K3C0GW5M57
  • DSSTox Substance ID:DTXSID50157593
  • Nikkaji Number:J14.259J
  • Wikipedia:1,2-Bis(dimethylarsino)benzene
  • Wikidata:Q3596745
  • Mol file:13246-32-7.mol
1,2-Bis(dimethylarsino)benzene

Synonyms:2-phenylene-bis-dimethylarsine;diArs

Suppliers and Price of 1,2-Bis(dimethylarsino)benzene
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
  • American Custom Chemicals Corporation
  • 1,2-PHENYLENEBIS(DIMETHYLARSINE) 98.00%
  • 1G
  • $ 1114.58
  • AHH
  • 1,2-Phenylenebis(dimethylarsine) 98%
  • 1g
  • $ 300.00
Total 9 raw suppliers
Chemical Property of 1,2-Bis(dimethylarsino)benzene
Chemical Property:
  • Vapor Pressure:0.013mmHg at 25°C 
  • Boiling Point:268°Cat760mmHg 
  • Flash Point:108.4°C 
  • PSA:0.00000 
  • Density:g/cm3 
  • LogP:1.60940 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:2
  • Exact Mass:285.96839
  • Heavy Atom Count:12
  • Complexity:116
Purity/Quality:

99% *data from raw suppliers

1,2-PHENYLENEBIS(DIMETHYLARSINE) 98.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C[As](C)C1=CC=CC=C1[As](C)C
  • General Description 1,2-PHENYLENEBIS(DIMETHYLARSINE) is an organoarsenic compound featuring a benzene ring substituted at the 1,2-positions with dimethylarsine groups. It is commonly referred to by various names, including 1,2-Bis(dimethylarsino)benzene and o-Phenylenebis(dimethylarsine). 1,2-PHENYLENEBIS(DIMETHYLARSINE) is known for its role as a chelating ligand in coordination chemistry, where it forms stable complexes with transition metals due to the presence of two arsenic donor atoms. Its applications are primarily in research settings, particularly in the synthesis of metal-organic frameworks or catalysts, though its toxicity and handling require careful consideration.
Technology Process of 1,2-Bis(dimethylarsino)benzene

There total 5 articles about 1,2-Bis(dimethylarsino)benzene 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:
Multistep reaction; (i) Na, THF, (ii) /BRN= 606078/;
DOI:10.1055/s-1974-23306
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