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Chloro(2,3-dihydro-1-benzofuran-2-ylmethyl)mercury

Base Information Edit
  • Chemical Name:Chloro(2,3-dihydro-1-benzofuran-2-ylmethyl)mercury
  • CAS No.:69914-63-2
  • Molecular Formula:C9H9HgO*Cl
  • Molecular Weight:369.213
  • Hs Code.:
  • NSC Number:513075
  • DSSTox Substance ID:DTXSID80331329
  • Mol file:69914-63-2.mol
Chloro(2,3-dihydro-1-benzofuran-2-ylmethyl)mercury

Synonyms:69914-63-2;chloro(2,3-dihydro-1-benzofuran-2-ylmethyl)mercury;NSC513075;SCHEMBL7826870;DTXSID80331329;NSC-513075

Suppliers and Price of Chloro(2,3-dihydro-1-benzofuran-2-ylmethyl)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 2 raw suppliers
Chemical Property of Chloro(2,3-dihydro-1-benzofuran-2-ylmethyl)mercury Edit
Chemical Property:
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:1
  • Exact Mass:370.004836
  • Heavy Atom Count:12
  • Complexity:154
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1C(OC2=CC=CC=C21)C[Hg]Cl
Technology Process of Chloro(2,3-dihydro-1-benzofuran-2-ylmethyl)mercury

There total 3 articles about Chloro(2,3-dihydro-1-benzofuran-2-ylmethyl)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:
With mercury dichloride; In not given; byproducts: HCl; treatment og HgCl2 soln. with o-allyl phenol at ambient temp.;;
DOI:10.1021/ja01429a024
Guidance literature:
With potassium chloride; In tetrahydrofuran; water; to a soln. of mercuric acetate in THF is added the olefin-compd. at room temp. under stirring for 3-5 h., a soln. of KCl in water is added and the soln. is stirred for 5 min.; the soln. is diluted with water and extracted with CH2Cl2, the extract is dried over anhydrous Na2SO4 and the solvent is evaporated under red. pressure, benzene is added to the residue and then evaporated, crystn. from AcOEt, purifn. by flash chromy.;
upstream raw materials:

o-Allylphenol

mercury(II) diacetate

Downstream raw materials:

(2,3-dihydro-2-benzofuranyl)-methyl bromide

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