N-[2-(4-Bromophenyl)-3H-indol-3-ylidene]benzenamine

Base Information

Chemical Name:N-[2-(4-Bromophenyl)-3H-indol-3-ylidene]benzenamine
CAS No.:142920-62-5
Molecular Formula:C₂₀H₁₃BrN₂
Molecular Weight:361.241
Hs Code.:
DSSTox Substance ID:DTXSID801223324

Synonyms:N-[2-(4-Bromophenyl)-3H-indol-3-ylidene]benzenamine;DTXSID801223324;142920-62-5

Suppliers and Price of N-[2-(4-Bromophenyl)-3H-indol-3-ylidene]benzenamine

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of N-[2-(4-Bromophenyl)-3H-indol-3-ylidene]benzenamine

Chemical Property:

XLogP3:5.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:360.02621
Heavy Atom Count:23
Complexity:470

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)N=C2C3=CC=CC=C3N=C2C4=CC=C(C=C4)Br

Technology Process of N-[2-(4-Bromophenyl)-3H-indol-3-ylidene]benzenamine

There total 3 articles about N-[2-(4-Bromophenyl)-3H-indol-3-ylidene]benzenamine 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: 70.0%

: 586-96-9
Nitrosobenzene

: 6127-49-7
2-(4-bromophenyl)indole

: 142920-62-5
2-(p-bromophenyl)-3-(phenylimino)-3H-indole

Guidance literature:: With sodium ethanolate; for 0.166667h; Heating;

Reference yield:

: 98-86-2
acetophenone

: 142920-62-5
2-(p-bromophenyl)-3-(phenylimino)-3H-indole

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / ZnCl₂ / 130 - 200 °C

2: 70 percent / ethanol. NaOEt / 0.17 h / Heating

With sodium ethanolate; zinc(II) chloride;

Reference yield:

: 589-21-9
(4-bromophenyl)hydrazine

: 142920-62-5
2-(p-bromophenyl)-3-(phenylimino)-3H-indole

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / ZnCl₂ / 130 - 200 °C

2: 70 percent / ethanol. NaOEt / 0.17 h / Heating

With sodium ethanolate; zinc(II) chloride;