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(Acetato-kappaO)(4-methoxyphenyl)mercury

Base Information Edit
  • Chemical Name:(Acetato-kappaO)(4-methoxyphenyl)mercury
  • CAS No.:5780-90-5
  • Molecular Formula:C9H10 Hg O3
  • Molecular Weight:366.767
  • Hs Code.:
  • DSSTox Substance ID:DTXSID10586769
  • NSC Number:61318
  • Mol file:5780-90-5.mol
(Acetato-kappaO)(4-methoxyphenyl)mercury

Synonyms:5780-90-5;(Acetato-kappaO)(4-methoxyphenyl)mercury;NCIOpen2_007908;DTXSID10586769;NSC61318;NSC-61318

Suppliers and Price of (Acetato-kappaO)(4-methoxyphenyl)mercury
Supply Marketing:Edit
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 4 raw suppliers
Chemical Property of (Acetato-kappaO)(4-methoxyphenyl)mercury Edit
Chemical Property:
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:4
  • Exact Mass:368.033638
  • Heavy Atom Count:13
  • Complexity:164
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(=O)O[Hg]C1=CC=C(C=C1)OC
Technology Process of (Acetato-kappaO)(4-methoxyphenyl)mercury

There total 2 articles about (Acetato-kappaO)(4-methoxyphenyl)mercury 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:
In not given; dried salt of Hg(II) acetate; on water bath;
Guidance literature:
In acetic acid; 250°C, dried salt of Hg(II) acetate; on water bath;
Guidance literature:
With palladium diacetate; In acetonitrile; for 12h; Ambient temperature;
DOI:10.1021/jo00262a014
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