Acetanilide, 2-indol-3-YL-

Base Information

Chemical Name:Acetanilide, 2-indol-3-YL-
CAS No.:52190-18-8
Molecular Formula:C16H14N2O
Molecular Weight:250.3
Hs Code.:2933990090
DSSTox Substance ID:DTXSID30200218
Nikkaji Number:J73.586H
Wikidata:Q83073279
Mol file:52190-18-8.mol

Synonyms:ACETANILIDE, 2-INDOL-3-YL-;52190-18-8;2-(1H-indol-3-yl)-N-phenylacetamide;N-Phenyl 3-indoleacetamide;3-Indoleacetamide, N-phenyl-;BRN 0221151;5-22-03-00070 (Beilstein Handbook Reference);(indol-3-yl)acetanilide;SCHEMBL7807900;2-(1H-Indol-3-yl)acetanilide;DTXSID30200218;AKOS001407607;Z27782686

Suppliers and Price of Acetanilide, 2-indol-3-YL-

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 Acetanilide, 2-indol-3-YL-

Chemical Property:

Vapor Pressure:4.86E-12mmHg at 25°C
Melting Point:186-187 °C(Solv: isopropanol (67-63-0))
Boiling Point:547.5°Cat760mmHg
PKA:14.98±0.70(Predicted)
Flash Point:284.9°C
PSA：48.38000
Density:1.279g/cm³
LogP:3.99860
XLogP3:2.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:250.110613074
Heavy Atom Count:19
Complexity:312

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)NC(=O)CC2=CNC3=CC=CC=C32

Technology Process of Acetanilide, 2-indol-3-YL-

There total 11 articles about Acetanilide, 2-indol-3-YL- 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: 95.0%

: 87-51-4
indole-3-acetic acid

: 62-53-3
aniline

: 52190-18-8
2-(1H-indol-3-yl)-N-phenyl acetamide

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 0 - 25 ℃; for 23h; Inert atmosphere;
DOI:10.1039/c2ob06695e

Reference yield: 70.0%

: N-(2-iodophenyl)-2-(1H-indol-3-yl)acetamide

: 52190-18-8
2-(1H-indol-3-yl)-N-phenyl acetamide

: 142273-18-5
paullone

Guidance literature:: With magnesium oxide; palladium diacetate; In N,N-dimethyl-formamide; at 130 ℃; for 24h;
DOI:10.1016/j.tetlet.2006.08.118

Reference yield: 60.0%

: 914929-95-6
N-(2-bromophenyl)-2-(1H-indol-3-yl)acetamide

: 52190-18-8
2-(1H-indol-3-yl)-N-phenyl acetamide

Guidance literature:: With potassium phosphate; palladium diacetate; In N,N-dimethyl-formamide; at 130 ℃; for 24h;
DOI:10.1016/j.tetlet.2006.08.118