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3-(2-oxo-2-phenylethyl)-1,3-dihydro-2H-indol-2-one is a complex organic compound with the molecular formula C16H13NO2. It is a derivative of indole, a heterocyclic aromatic organic compound that contains a benzene ring fused to a pyrrole. This specific compound features a 2-phenylethyl group attached to the indole nucleus, with an oxo group (carbonyl) at the 2-position of the phenylethyl chain. The compound is characterized by its 1,3-dihydro structure, indicating that it has two hydrogen atoms added across a double bond, and a 2H-indol-2-one functional group, which is an indole with a ketone group at the 2-position. This chemical structure may be relevant in various applications, such as pharmaceuticals or materials science, due to its unique properties and potential reactivity.

842-27-3

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842-27-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 842-27-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,4 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 842-27:
(5*8)+(4*4)+(3*2)+(2*2)+(1*7)=73
73 % 10 = 3
So 842-27-3 is a valid CAS Registry Number.

842-27-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenacyl-1,3-dihydroindol-2-one

1.2 Other means of identification

Product number -
Other names 3-Benzoylmethyl-oxindol

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:842-27-3 SDS

842-27-3Relevant academic research and scientific papers

Synthesis of Annulated Carbazoles from Indol-2,3-dione

Beccalli, Egle M.,Marchesini, Alessandro,Pilati, Tullio

, p. 4741 - 4758 (2007/10/02)

Reaction of ethyl chloroformate with 3-aroylmethylindol-2(3H)-ones 5 affords the ethyl 3--2-(ethoxycarbonyloxy)indole-1-carboxylates 6 from which the corresponding annulated carbazoles 10 are obtained via 6?-electro

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