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2H-Indol-2-one, 1-(azidoacetyl)-1,3-dihydro-3,3-dimethyl- is a complex organic compound with the chemical formula C11H12N4O2. It is a derivative of indol-2-one, featuring an azidoacetyl group attached to the 1-position and two methyl groups at the 3-position. This molecule is of interest in chemical research due to its unique structure and potential applications in the synthesis of various pharmaceuticals and agrochemicals. Its properties, such as reactivity and stability, are influenced by the presence of the azido group, which can participate in various chemical reactions, making it a valuable building block in organic synthesis.

910562-92-4

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910562-92-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 910562-92-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,0,5,6 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 910562-92:
(8*9)+(7*1)+(6*0)+(5*5)+(4*6)+(3*2)+(2*9)+(1*2)=154
154 % 10 = 4
So 910562-92-4 is a valid CAS Registry Number.

910562-92-4SDS

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 2H-Indol-2-one, 1-(2-azidoacetyl)-1,3-dihydro-3,3-dimethyl-

1.2 Other means of identification

Product number -
Other names 2H-Indol-2-one, 1-(azidoacetyl)-1,3-dihydro-3,3-dimethyl-

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:910562-92-4 SDS

910562-92-4Downstream Products

910562-92-4Relevant academic research and scientific papers

Spiroquinazoline support studies: methods for the preparation of imidazoloindolines from oxindoles

Ortiz Barbosa, Yomadis A.,Hart, David J.,Magomedov, Nabi A.

, p. 8748 - 8754 (2006)

Two methods for the annulation of glycine to the 1 and 2 positions of oxindoles are described. The first method involves introduction of an α-azidoacetyl group on the oxindole nitrogen followed by an intramolecular Staudinger reaction to complete the annu

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