phenylmercury thiobenzoate

Base Information

Chemical Name:phenylmercury thiobenzoate
CAS No.:79293-05-3
Molecular Formula:C₁₃H₁₀HgOS
Molecular Weight:414.878
Hs Code.:

Synonyms:phenylmercury thiobenzoate

Suppliers and Price of phenylmercury thiobenzoate

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 0 raw suppliers

Chemical Property of phenylmercury thiobenzoate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of phenylmercury thiobenzoate

There total 1 articles about phenylmercury thiobenzoate 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:

Reference yield: 91.0%

: 98-91-9
thiobenzoic acid

: 587-85-9,1337-09-3
diphenylmercury(II)

: 79293-05-3
phenylmercury thiobenzoate

Guidance literature:: In benzene; byproducts: C6H6; HgPh2 is added to a soln. of the acid in benzene, refluxed; the solvent is evapd. in vac., the residue is washed (n-hexane), recrystd. (CH2Cl2/n-hexane), elem. anal.;

Reference yield: 85.0%

: 79293-05-3
phenylmercury thiobenzoate

: 85156-87-2
Benzoylsulfenyl bromide

Guidance literature:: With N-Bromosuccinimide; In chloroform; for 0.5h; Ambient temperature;
DOI:10.1055/s-1982-30042

Reference yield:

: 79293-05-3
phenylmercury thiobenzoate

: 644-32-6
dibenzoyl disulfide

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / NBS / CHCl₃ / 0.5 h / Ambient temperature

2: 99 percent / 0.25 h / Ambient temperature; Irradiation

With N-Bromosuccinimide; In chloroform;
DOI:10.1055/s-1982-30042