1H-Indole,3,3'-[2-(2-nitrophenyl)ethylidene]bis-

Base Information

Chemical Name:1H-Indole,3,3'-[2-(2-nitrophenyl)ethylidene]bis-
CAS No.:7479-22-3
Molecular Formula:C₂₄H₁₉N₃O₂
Molecular Weight:381.434
Hs Code.:

Synonyms:Indole,3,3'-(o-nitrophenethylidene)di- (6CI); Indole,3,3'-[2-(o-nitrophenyl)ethylidene]di- (8CI); NSC 401602

Suppliers and Price of 1H-Indole,3,3'-[2-(2-nitrophenyl)ethylidene]bis-

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 6 raw suppliers

Chemical Property of 1H-Indole,3,3'-[2-(2-nitrophenyl)ethylidene]bis-

Chemical Property:

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1H-Indole,3,3'-[2-(2-nitrophenyl)ethylidene]bis-

There total 4 articles about 1H-Indole,3,3'-[2-(2-nitrophenyl)ethylidene]bis- 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: 0.82%

: 120-72-9
indole

: 1969-73-9
(2-nitrophenyl)acetaldehyde

: 7479-22-3
3,3'-(o-nitrophenethylidene)di-indole

Guidance literature:: In acetic acid; at 105 ℃; for 2h;

Reference yield:

: 120-72-9
indole

: 1969-73-9
(2-nitrophenyl)acetaldehyde

: 7479-22-3
3,3'-(o-nitrophenethylidene)di-indole

: 117768-67-9
2,3'-(o-nitrophenethylidene)di-indole

Guidance literature:: With zinc(II) chloride; In acetic acid; at 105 ℃; for 2h;

Reference yield:

: 15582-86-2
methyl o-nitrostyrylcarbamate

: 7479-22-3
3,3'-(o-nitrophenethylidene)di-indole

Guidance literature:: Multi-step reaction with 2 steps

1: 0.19 percent / 20 percent H₂SO₄ / 1 h / Heating

2: 0.82 percent / acetic acid / 2 h / 105 °C

With sulfuric acid; In acetic acid;