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3-[hydroxy(methyl)amino]-2H-indol-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58418-20-5

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58418-20-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58418-20-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,4,1 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 58418-20:
(7*5)+(6*8)+(5*4)+(4*1)+(3*8)+(2*2)+(1*0)=135
135 % 10 = 5
So 58418-20-5 is a valid CAS Registry Number.

58418-20-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[hydroxy(methyl)amino]indol-2-one

1.2 Other means of identification

Product number -
Other names -

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:58418-20-5 SDS

58418-20-5Downstream Products

58418-20-5Relevant academic research and scientific papers

Structure, Anticorrosion and Antibacterial Evaluation of (E)-3-(N-Oxide-methylimino)indolin-2-one

Bai, Li,Feng, Lajun,Yan, Jiao,Lin, Jiao,Zhang, Jie,Ma, Yun,Gu, Xuefan,Chen, Gang

, (2018)

A nitrone, (E)-3-(N-oxide-methylimino)indolin-2-one, was synthesized and analyzed by X-ray single crystal analysis. The inhibition and the mechanism of action of the title compound on the corrosion of high protective Q235A steel in HCl solution were scree

Nitrones and nucleobase-containing spiro-isoxazolidines derived from isatin and indanone: Solvent-free microwave-assisted stereoselective synthesis and theoretical calculations

Maiuolo, Loredana,Merino, Pedro,Algieri, Vincenzo,Nardi, Monica,Di Gioia, Maria Luisa,Russo, Beatrice,Delso, Ignacio,Tallarida, Matteo Antonio,De Nino, Antonio

, p. 48980 - 48988 (2017/11/06)

The spiro-oxindoles have found wide application because of their antiviral properties. However, in the literature few examples of synthesis of their precursors, oxindole-nitrones, are reported. In this paper, we initially present a rapid and efficient synthetic approach to ketonitrones by solvent-free microwave-assisted reaction between isatin or indanone derivatives and various hydroxylamines. The synthetic protocol is facile, clean, fast, high-yielding and stereoselective. Then, we explored the possibility to synthesize nucleobase-containing spiro-isoxazolidines with isatin and indanone nuclei by solvent-free MW-assisted 1,3-dipolar cycloaddition, obtaining good results in yields (74-85%), and regio- and diastereoselectivity. Theoretical calculations were done to analyze the difference of reactivity of isatin and indanone derivatives with hydroxylamines.

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