5-Methyl-2-phenyl-1H-indol-3-amine

Base Information

Chemical Name:5-Methyl-2-phenyl-1H-indol-3-amine
CAS No.:23747-09-3
Molecular Formula:C15H14N2
Molecular Weight:222.28500
Hs Code.:
DSSTox Substance ID:DTXSID70574748
Mol file:23747-09-3.mol

Synonyms:5-Methyl-2-phenyl-1H-indol-3-amine;23747-09-3;DTXSID70574748

Suppliers and Price of 5-Methyl-2-phenyl-1H-indol-3-amine

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 5-Methyl-2-phenyl-1H-indol-3-amine

Chemical Property:

Boiling Point:447.4±40.0 °C(Predicted)
PSA：41.81000
Density:1.196±0.06 g/cm3(Predicted)
LogP:4.30670
XLogP3:3.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:222.115698455
Heavy Atom Count:17
Complexity:260

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC2=C(C=C1)NC(=C2N)C3=CC=CC=C3

Technology Process of 5-Methyl-2-phenyl-1H-indol-3-amine

There total 2 articles about 5-Methyl-2-phenyl-1H-indol-3-amine 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:

: 105492-07-7
5-Methyl-3-nitroso-2-phenyl-1H-indole

: 23747-09-3
5-Methyl-2-phenyl-3-aminoindole

Guidance literature:: With sodium hydroxide; sodium dithionite; In ethanol; Heating;

Reference yield:

: 13228-36-9
5-methyl-2-phenyl-1H-indole

: 23747-09-3
5-Methyl-2-phenyl-3-aminoindole

Guidance literature:: Multi-step reaction with 2 steps

1: sodium nitrite, acetic acid / H₂O / 0.5 h / Ambient temperature

2: 2N NaOH, sodium dithionite / ethanol / Heating

With sodium hydroxide; sodium dithionite; acetic acid; sodium nitrite; In ethanol; water;