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2H-Indol-2-one, 1,3-dihydro-1,3,3-triphenyl- is a complex organic compound with the chemical formula C25H19NO. It is a derivative of indol-2-one, featuring a 1,3-dihydro structure and three phenyl groups attached to the molecule. 2H-Indol-2-one, 1,3-dihydro-1,3,3-triphenyl- is known for its potential applications in pharmaceutical research and the synthesis of various biologically active molecules. Its structure provides a stable platform for further chemical modifications, making it a valuable intermediate in the development of new drugs and other chemical entities.

124145-27-3

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124145-27-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124145-27-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,1,4 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 124145-27:
(8*1)+(7*2)+(6*4)+(5*1)+(4*4)+(3*5)+(2*2)+(1*7)=93
93 % 10 = 3
So 124145-27-3 is a valid CAS Registry Number.

124145-27-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,3-triphenylindol-2-one

1.2 Other means of identification

Product number -
Other names 1,3,3-triphenyl-indolin-2-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:124145-27-3 SDS

124145-27-3Downstream Products

124145-27-3Relevant academic research and scientific papers

Multiple Aryne Insertions into Oxindoles: Synthesis of Bioactive 3,3-Diarylated Oxindoles and Dibenzo[b,e]azepin-6-ones

Samineni, Ramesh,Bandi, Chandramohan Reddy C.,Srihari, Pabbaraja,Mehta, Goverdhan

supporting information, p. 6184 - 6187 (2016/12/09)

An aryne insertion cascade reaction on oxindoles has been observed and constitutes a convenient one pot preparation of bioactive di- and triarylated oxindoles in good yields under mild conditions. A temperature controlled reaction switch enables ready access to dibenzo[b,e]azepin-6-one derivatives employing the same reaction regime. This tactic has been extended to a short synthesis of potent antiulcer agent darenzepine.

Transition metal and base-free synthesis of 3,3-diaryl-2-oxindoles from 2,2,N-triarylacetamides

Lim, Jin Woo,Kim, Ko Hoon,Moon, Hye Ran,Kim, Jae Nyoung

supporting information, p. 784 - 787 (2016/02/03)

A transition metal and base-free synthesis of 3,3-diaryl-2-oxindoles has been developed from 2,2,N-triarylacetamides in the presence of montmorillonite K-10 in 1,2-dichlorobenzene under O2 balloon atmosphere.

α-Arylation of oxindoles using recyclable metal oxide ferrite nanoparticles: Comparison between the catalytic activities of nickel, cobalt and copper ferrite nanoparticles

Moghaddam, Firouz Matloubi,Tavakoli, Ghazal,Latifi, Fatemeh,Saeednia, Borna

, p. 37 - 41 (2015/12/24)

Three different spinel metal oxide catalytic systems including NiFe2O4, CuFe2O4 and CoFe2O4 were synthesized using co-precipitation technique and their catalytic activities were compared to

3-3-DI-SUBSTITUTED-OXINDOLES AS INHIBITORS OF TRANSLATION INITIATION

-

Page/Page column 32, (2008/06/13)

Compositions and methods for inhibiting translation using 3-(5-tert-Butyl-2-Hydroxy-phenyl)-3-phenyl-1,3-dihydro-indol-2-one and/or its derivatives are provided. Compositions, methods and kits for treating (1) cellular proliferative disorders, (2) non-proliferative, degenerative disorders, (3) viral infections, and/or (4) disorders associated with viral infections, using 3-(5-tert-butyl-2-hydroxy-phenyl)-3-phenyl-1,3-dihydro-indol-2-one and/or its derivatives are described.

Preparation of 3,3-Diaryloxindoles by superacid-induced condensations of isatins and aromatics with a combinatorial approach

Klumpp, Douglas A.,Yeung, Ka Yeun,Prakash, G.K. Surya,Olah, George A.

, p. 4481 - 4484 (2007/10/03)

3,3-Diaryloxidoles are prepared in high yields (62-99%) by reaction of isatin or substituted isatins with aromatics in triflic acid. The reaction shows a significant dependence on acid strength which suggests the formation of diprotonated, superelectrophi

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