3H-Indole, 3-(1-oxido-2-phenyl-3H-indol-3-ylidene)-2-phenyl-, 1-oxide

Base Information

Chemical Name:3H-Indole, 3-(1-oxido-2-phenyl-3H-indol-3-ylidene)-2-phenyl-, 1-oxide
CAS No.:2196-95-4
Molecular Formula:C₂₈H₁₈N₂O₂
Molecular Weight:414.463
Hs Code.:
Mol file:2196-95-4.mol

Synonyms:

Suppliers and Price of 3H-Indole, 3-(1-oxido-2-phenyl-3H-indol-3-ylidene)-2-phenyl-, 1-oxide

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 5 raw suppliers

Chemical Property of 3H-Indole, 3-(1-oxido-2-phenyl-3H-indol-3-ylidene)-2-phenyl-, 1-oxide

Chemical Property:

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 3H-Indole, 3-(1-oxido-2-phenyl-3H-indol-3-ylidene)-2-phenyl-, 1-oxide

There total 7 articles about 3H-Indole, 3-(1-oxido-2-phenyl-3H-indol-3-ylidene)-2-phenyl-, 1-oxide 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: 97.0%

: 1859-39-8
2-phenyl-N-hydroxyindole

: 2196-95-4,17213-48-8
2,2'-diphenyl-[3,3']biindolylidene 1,1'-dioxide

Guidance literature:: With dihydrogen peroxide; calcium chloride; In methanol; at 70 ℃; for 4h;
DOI:10.1039/b102915k

Reference yield: 57.0%

: 1859-39-8
2-phenyl-N-hydroxyindole

: 1969-74-0
2-phenylisatogen

: 2196-95-4,17213-48-8
2,2'-diphenyl-[3,3']biindolylidene 1,1'-dioxide

Guidance literature:: With dipotassium peroxodisulfate; In water; acetonitrile; for 24h; Product distribution; Mechanism; Ambient temperature; other oxidant (36 percent H₂O₂) and time;