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Arsabenzene

Base Information
  • Chemical Name:Arsabenzene
  • CAS No.:289-31-6
  • Molecular Formula:C5H5 As
  • Molecular Weight:140.016
  • Hs Code.:
  • DSSTox Substance ID:DTXSID90183093
  • Nikkaji Number:J11.600I
  • Wikipedia:Arsabenzene
  • Wikidata:Q1057745
  • Mol file:289-31-6.mol
Arsabenzene

Synonyms:arsabenzene

Suppliers and Price of Arsabenzene
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
Total 5 raw suppliers
Chemical Property of Arsabenzene
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:0.00000 
  • Density:g/cm3 
  • LogP:0.57630 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:0
  • Exact Mass:139.960720
  • Heavy Atom Count:6
  • Complexity:30.9
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=[As]C=C1
  • General Description 1-Arsabenzene, also known as arsabenzene, is an arsenic-containing aromatic heterocycle where one carbon atom in the benzene ring is replaced by an arsenic atom. It exhibits aromaticity due to the delocalization of π-electrons across the ring, similar to benzene, but with distinct electronic and reactivity properties influenced by the arsenic heteroatom. 1-Arsabenzene is of interest in organoarsenic chemistry and materials science for its unique structural and electronic characteristics.
Technology Process of Arsabenzene

There total 6 articles about Arsabenzene 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 arsenic trichloride; In tetrahydrofuran;
DOI:10.1016/S0022-328X(00)90981-1
Guidance literature:
With arsenic trichloride; In tetrahydrofuran;
DOI:10.1016/S0022-328X(00)90981-1
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