2-Phenyl-1,3,2-dithiastibolane

Base Information

Chemical Name:2-Phenyl-1,3,2-dithiastibolane
CAS No.:51525-64-5
Molecular Formula:C8H9S2Sb
Molecular Weight:291.041
Hs Code.:
DSSTox Substance ID:DTXSID00587200
Wikidata:Q82479553

Synonyms:2-Phenyl-1,3,2-dithiastibolane;51525-64-5;DTXSID00587200

Suppliers and Price of 2-Phenyl-1,3,2-dithiastibolane

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 2-Phenyl-1,3,2-dithiastibolane

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:289.91838
Heavy Atom Count:11
Complexity:117

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CS[Sb](S1)C2=CC=CC=C2

Technology Process of 2-Phenyl-1,3,2-dithiastibolane

There total 7 articles about 2-Phenyl-1,3,2-dithiastibolane 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: 53.0%

: 5035-52-9
dichlorophenylstibine

: 540-63-6
ethane-1,2-dithiol

: 121-44-8
triethylamine

: 51525-64-5
C₆H₅Sb(SCH₂CH₂S)

Guidance literature:: In benzene; byproducts: {(C2H5)3NH}Cl; stirring; ppt. is filtered off and the filtrate concd.;

Reference yield: 50.0%

: 5035-52-9
dichlorophenylstibine

: 540-63-6
ethane-1,2-dithiol

: 51525-64-5
C₆H₅Sb(SCH₂CH₂S)

Guidance literature:: With triethylamine; In benzene;

Reference yield:

: phenyl antimony ⁽⁴⁺⁾; tetrachloride

: 51525-64-5
C₆H₅Sb(SCH₂CH₂S)

Guidance literature:: Multi-step reaction with 2 steps

1: SO₂ / potassium iodide

2: N(C₂H₅)3 / benzene

With SO₂; N(C₂H₅)3; potassium iodide; In benzene;