3H-Indol-2-amine, 3,3-diphenyl-

Base Information

Chemical Name:3H-Indol-2-amine, 3,3-diphenyl-
CAS No.:61352-09-8
Molecular Formula:C20H16N2
Molecular Weight:284.36
Hs Code.:
DSSTox Substance ID:DTXSID30432875
Wikidata:Q82246997

Synonyms:3,3-Diphenyl-3H-indol-2-amine;61352-09-8;3H-Indol-2-amine, 3,3-diphenyl-;SCHEMBL6550923;DTXSID30432875

Suppliers and Price of 3H-Indol-2-amine, 3,3-diphenyl-

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 3 raw suppliers

Chemical Property of 3H-Indol-2-amine, 3,3-diphenyl-

Chemical Property:

XLogP3:3.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:284.131348519
Heavy Atom Count:22
Complexity:397

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2(C3=CC=CC=C3N=C2N)C4=CC=CC=C4

Technology Process of 3H-Indol-2-amine, 3,3-diphenyl-

There total 5 articles about 3H-Indol-2-amine, 3,3-diphenyl- 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: 88.0%

: 143-33-9,25596-52-5
sodium cyanide

: 82757-19-5
2-formamidotriphenylmethanol

: 61352-09-8
2-amino-3,3-diphenyl-3H-indolenine

Guidance literature:: In N,N-dimethyl-formamide; at 80 ℃; for 28h;

Reference yield:

: 10113-38-9
N-(2-bromophenyl)formamide

: 61352-09-8
2-amino-3,3-diphenyl-3H-indolenine

Guidance literature:: Multi-step reaction with 3 steps

1: n-butyl lithium / hexane; tetrahydrofuran / -100 °C

2: 56 percent / tetrahydrofuran / -105 °C

3: 88 percent / dimethylformamide / 80 °C

With n-butyllithium; In tetrahydrofuran; hexane; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(00)87259-7

Reference yield:

: 119-61-9
benzophenone

: 61352-09-8
2-amino-3,3-diphenyl-3H-indolenine

Guidance literature:: Multi-step reaction with 2 steps

1: 56 percent / tetrahydrofuran / -105 °C

2: 88 percent / dimethylformamide / 80 °C

In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(00)87259-7