5,5'-Thiobis(2-phenylisoindoline-1,3-dione)

Base Information

Chemical Name:5,5'-Thiobis(2-phenylisoindoline-1,3-dione)
CAS No.:58974-89-3
Molecular Formula:C28H16N2O4S
Molecular Weight:476.512
Hs Code.:
DSSTox Substance ID:DTXSID50551335
Wikidata:Q82430939
Mol file:58974-89-3.mol

Synonyms:5,5'-Thiobis(2-phenylisoindoline-1,3-dione);58974-89-3;5-(1,3-dioxo-2-phenylisoindol-5-yl)sulfanyl-2-phenylisoindole-1,3-dione;5,5'-Thiobis[2-phenyl-1H-isoindole-1,3(2H)-dione];5-[(1,3-dioxo-2-phenyl-2,3-dihydro-1H-isoindol-5-yl)sulfanyl]-2-phenyl-2,3-dihydro-1H-isoindole-1,3-dione;SCHEMBL9580861;DTXSID50551335;BYIRGVINJRTNPE-UHFFFAOYSA-N;4,4'-thiobis(N-phenylphthalimide);H11609;5,5'-Sulfanediylbis(2-phenyl-1H-isoindole-1,3(2H)-dione)

Suppliers and Price of 5,5'-Thiobis(2-phenylisoindoline-1,3-dione)

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

Chemenu
5,5''-thiobis(2-phenylisoindoline-1,3-dione) 95%+
10g
$ 608.00

Chemenu
5,5''-thiobis(2-phenylisoindoline-1,3-dione) 95%+
5g
$ 365.00

Alichem
5,5'-Thiobis(2-phenylisoindoline-1,3-dione)
10g
$ 676.00

Total 6 raw suppliers

Chemical Property of 5,5'-Thiobis(2-phenylisoindoline-1,3-dione)

Chemical Property:

PSA：100.06000
LogP:5.56900
XLogP3:5.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:476.08307817
Heavy Atom Count:35
Complexity:810

Purity/Quality:

99% ^*data from raw suppliers

5,5''-thiobis(2-phenylisoindoline-1,3-dione) 95%+ ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)N2C(=O)C3=C(C2=O)C=C(C=C3)SC4=CC5=C(C=C4)C(=O)N(C5=O)C6=CC=CC=C6

Technology Process of 5,5'-Thiobis(2-phenylisoindoline-1,3-dione)

There total 4 articles about 5,5'-Thiobis(2-phenylisoindoline-1,3-dione) 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: 95.0%