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1H-Indole-2,3-dione, 5-methoxy-, 3-oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

109103-45-9

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109103-45-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109103-45-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,1,0 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 109103-45:
(8*1)+(7*0)+(6*9)+(5*1)+(4*0)+(3*3)+(2*4)+(1*5)=89
89 % 10 = 9
So 109103-45-9 is a valid CAS Registry Number.

109103-45-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(hydroxyamino)-5-methoxyindol-2-one

1.2 Other means of identification

Product number -
Other names (3Z)-3-(hydroxyimino)-5-methoxy-2,3-dihydro-1H-indol-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:109103-45-9 SDS

109103-45-9Relevant academic research and scientific papers

Metal-free synthesis of isatin oximes: Via radical coupling reactions of oxindoles with t -BuONO in water

Wei, Wen-Ting,Zhu, Wen-Ming,Ying, Wei-Wei,Wu, Yi,Huang, Yi-Ling,Liang, Hongze

, p. 5254 - 5257 (2017)

A metal-free method for the synthesis of isatin oximes was developed through the radical coupling reactions of oxindoles with t-BuONO. This protocol provides a practical and environmentally benign method for the construction of C-N bonds in water at room temperature without using any other reagents. The advantages of this strategy are its mild reaction conditions and clean procedure.

KINASE INHIBITORS AND METHOD OF TREATING CANCER WITH SAME

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Page/Page column 27, (2011/10/31)

The invention is directed to a compound represented by the following structural formula pharmaceutically acceptable salts thereof: (I). Compounds represented by this structural formula are kinase inhibitors and are therefore disclosed herein for the treatment of cancer. Definitions for the variables in the structural formula are provided herein.

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