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2,3-Dioxoindoline-5-carboxamide, with the molecular formula C9H6N2O3, is a heterocyclic compound that features an indole ring fused with a carboxamide group. This chemical entity is recognized for its role in organic synthesis, particularly as a building block for the creation of pharmaceuticals and agrochemicals. Its biological activity and potential as a drug candidate for treating various diseases, such as cancer and infectious diseases, highlight its significance in the field of medicinal chemistry. Additionally, it finds applications in coordination chemistry as a ligand and in chemical reactions for synthesizing complex organic molecules.

28283-98-9

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28283-98-9 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
2,3-Dioxoindoline-5-carboxamide is utilized as a key building block for the synthesis of various pharmaceuticals and agrochemicals. Its unique structure and reactivity contribute to the development of new compounds with therapeutic and pesticidal properties, respectively.
Used in Medicinal Chemistry Research:
As a drug candidate, 2,3-Dioxoindoline-5-carboxamide is employed in the research and development of treatments for a range of diseases, including cancer and infectious diseases. Its biological activity makes it a promising candidate for further investigation and potential clinical applications.
Used in Coordination Chemistry:
2,3-Dioxoindoline-5-carboxamide serves as a ligand in coordination chemistry, where it forms complexes with metal ions. These complexes can exhibit unique properties and applications, such as in catalysis or as functional materials.
Used in Organic Synthesis as a Reagent:
In chemical reactions, 2,3-Dioxoindoline-5-carboxamide acts as a reagent for the synthesis of complex organic molecules. Its ability to participate in various types of chemical transformations makes it a valuable tool in the synthesis of intricate organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 28283-98-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,8 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 28283-98:
(7*2)+(6*8)+(5*2)+(4*8)+(3*3)+(2*9)+(1*8)=139
139 % 10 = 9
So 28283-98-9 is a valid CAS Registry Number.

28283-98-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dioxo-1H-indole-5-carboxamide

1.2 Other means of identification

Product number -
Other names 1H-indole-2,3-dione-5-carboxylic acid amide

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:28283-98-9 SDS

28283-98-9Relevant academic research and scientific papers

Potent inhibitors of SARS-CoV-2 3C-like protease derived from N-substituted isatin compounds

Liu, Pei,Liu, Hongbo,Sun, Qi,Liang, Hao,Li, Chunmei,Deng, Xiaobing,Liu, Ying,Lai, Luhua

, (2020/08/14)

SARS-CoV-2 3C-like protease is the main protease of SARS-CoV-2 and has been considered as one of the key targets for drug discovery against COVID-19. We identified several N-substituted isatin compounds as potent SARS-CoV-2 3C-like protease inhibitors. Th

Isatin compounds as noncovalent SARS coronavirus 3C-like protease inhibitors

Zhou, Lu,Liu, Ying,Zhang, Weilin,Wei, Ping,Huang, Changkang,Pei, Jianfeng,Yuan, Yaxia,Lai, Luhua

, p. 3440 - 3443 (2007/10/03)

A series of isatin derivatives were synthesized and tested against SARS CoV 3C-like protease. Substitutions at the N-1 and C-5 positions were examined to elucidate the differences in substrate binding sites of the rhinovirus 3C protease and SARS CoV 3C-li

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