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3-(Pyridin-3-yl-methyl)indolin-2-one is a chemical compound with the molecular formula C14H12N2O. It is a derivative of indolin-2-one, featuring a pyridin-3-yl-methyl group attached to the 3-position of the indoline ring. 3-(pyridin-3-yl-methyl)indolin-2-one is known for its potential applications in medicinal chemistry, particularly as a building block for the synthesis of various biologically active molecules. Its structure allows for the exploration of different chemical modifications, which can lead to the development of new drugs with improved pharmacological properties. The compound's synthesis and reactivity have been studied to understand its role in the formation of complex molecular architectures, making it an interesting subject for researchers in the field of organic chemistry and drug discovery.

3367-85-9

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3367-85-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3367-85-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,6 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3367-85:
(6*3)+(5*3)+(4*6)+(3*7)+(2*8)+(1*5)=99
99 % 10 = 9
So 3367-85-9 is a valid CAS Registry Number.

3367-85-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(pyridin-3-yl-methyl)indolin-2-one

1.2 Other means of identification

Product number -
Other names 2-Oxo-3-<pyridyl-(3)-methyl>-2.3-dihydro-indol

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

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More Details:3367-85-9 SDS

3367-85-9Downstream Products

3367-85-9Relevant academic research and scientific papers

Iridium catalysed C-3 alkylation of oxindole with alcohols under solvent free thermal or microwave conditions

Grigg, Ronald,Whitney, Simon,Sridharan, Visuvanathar,Keep, Ann,Derrick, Andrew

experimental part, p. 4375 - 4383 (2009/10/17)

Ir-catalysed alkylation of oxindole and N-methyl oxindole with a range of substituted benzyl and heteroaryl alcohols under solvent free thermal or microwave conditions afforded the corresponding C-3-monoalkylated products in high to excellent yield.

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