1H-Indole, 1,3-dibenzoyl-

Base Information

Chemical Name:1H-Indole, 1,3-dibenzoyl-
CAS No.:67060-92-8
Molecular Formula:C22H15NO2
Molecular Weight:325.367
Hs Code.:
DSSTox Substance ID:DTXSID70441224
Nikkaji Number:J1.086.481J
Wikidata:Q82257894

Synonyms:1H-Indole, 1,3-dibenzoyl-;1,3-dibenzoylindole;1,3-Dibenzoyl-1H-indole;67060-92-8;DTXSID70441224

Suppliers and Price of 1H-Indole, 1,3-dibenzoyl-

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 1 raw suppliers

Chemical Property of 1H-Indole, 1,3-dibenzoyl-

Chemical Property:

XLogP3:4.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:325.110278721
Heavy Atom Count:25
Complexity:490

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)C2=CN(C3=CC=CC=C32)C(=O)C4=CC=CC=C4

Technology Process of 1H-Indole, 1,3-dibenzoyl-

There total 21 articles about 1H-Indole, 1,3-dibenzoyl- 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: 85.0%

: 15224-25-6
3-benzoylindole

: 98-88-4
benzoyl chloride

: 67060-92-8
(1H-indole-1,3-diyl)bis(phenylmethanone)

Guidance literature:: With sodium hydroxide; tetraethylammonium bromide; In dichloromethane; at 0 ℃; for 0.5h;

Reference yield: 49.0%

: 93-97-0
benzoic acid anhydride

: [3-(2-aminophenyl)prop-2-enyl]triphenylphosphonium bromide

: 67060-92-8
(1H-indole-1,3-diyl)bis(phenylmethanone)

Guidance literature:: With N-ethyl-N,N-diisopropylamine; at 120 ℃; for 18h;
DOI:10.1016/S0040-4039(02)02199-8

Reference yield: 32.0%

: 1496-76-0
N-benzoylindole

: 611-73-4
Benzoylformic acid

: (1H-indole-1,2-diyl)bis(phenylmethanone)

: 67060-92-8
(1H-indole-1,3-diyl)bis(phenylmethanone)

Guidance literature:: With [Fe(ethylenediaminetetraacetate)]^(1-); dihydrogen peroxide; palladium diacetate; sodium hydroxide; In water; at 20 ℃; pH=7.2 - 7.8;
DOI:10.1002/adsc.201201085