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2(1H)-Pyridinone,4-hydrazino-(9CI) is a chemical compound with the molecular formula C5H7N3O. It is a derivative of pyridine and contains a hydrazino group, which consists of a nitrogen atom doubly bonded to another nitrogen atom. 2(1H)-Pyridinone,4-hydrazino-(9CI) is known for its potential applications in various fields, including pharmaceutical and agrochemical industries, organic synthesis, and materials science. Its unique properties and reactivity make it a versatile building block for the synthesis of various compounds and materials. Further research and development of 2(1H)-Pyridinone,4-hydrazino-(9CI) may lead to the discovery of new applications and uses in different fields.

106689-41-2

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106689-41-2 Usage

Uses

Used in Pharmaceutical Industry:
2(1H)-Pyridinone,4-hydrazino-(9CI) is used as a building block for the synthesis of pharmaceutical compounds. Its unique structure and reactivity allow for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 2(1H)-Pyridinone,4-hydrazino-(9CI) is used as a precursor for the synthesis of agrochemicals, such as pesticides and herbicides. Its versatile chemical properties enable the creation of effective and targeted agrochemicals.
Used in Organic Synthesis:
2(1H)-Pyridinone,4-hydrazino-(9CI) is used as a versatile building block in organic synthesis. Its reactivity and unique structure make it suitable for the synthesis of a wide range of organic compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Materials Science:
In materials science, 2(1H)-Pyridinone,4-hydrazino-(9CI) is used for the development of new materials with specific properties. Its unique chemical structure and reactivity contribute to the creation of advanced materials with potential applications in various industries, such as electronics, coatings, and adhesives.
As research and development in these fields continue, the potential applications and uses of 2(1H)-Pyridinone,4-hydrazino-(9CI) may expand, leading to new discoveries and innovations in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 106689-41-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,6,8 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 106689-41:
(8*1)+(7*0)+(6*6)+(5*6)+(4*8)+(3*9)+(2*4)+(1*1)=142
142 % 10 = 2
So 106689-41-2 is a valid CAS Registry Number.

106689-41-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Hydrazinylpyridin-2(1H)-one

1.2 Other means of identification

Product number -
Other names 4-hydrazinyl-1H-pyridin-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:106689-41-2 SDS

106689-41-2Relevant academic research and scientific papers

A COMPOSITION FOR TREATING OR PREVENTING A CANCER COMPRISING PYRROLOPYRIDINE DERIVATIVES

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Page/Page column 15, (2010/11/25)

The present invention provides a composition for treating or preventing a cancer comprising a pyrrolopyridine derivative or its salt and a pharmaceutically acceptable carrier.

PYRROLO[3,2-c]PYRIDINE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF

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Page/Page column 11, (2008/06/13)

The present invention provides novel pyrrolo[3,2-c]pyridine derivatives or pharmaceutically acceptable salts thereof, processes for the preparation thereof, and compositions comprising the same. The pyrrolo[3,2-c]pyridine derivatives or pharmaceutically a

AUTRE VOIE D'ACCES AUX 5H-PYRIDOPYRROLOPYRIDINES ET LEUR TRANSFORMATION EN DERIVES N-5 ET N-8 SUBSTITUES

Hung, Nguyen Chi,Bisagni, Emile

, p. 2303 - 2310 (2007/10/02)

4-hydrazino-1H-pyridin-2-ones obtained starting from corresponding 2,4-dihydroxypiridines react with N-acetyl 4-piperidone.The expected hydrazones then give 6,7,8,9-tetrahydro 8-acetyl-2H,5H-pyridopyrrolopyridin-1-ones by thermal Fischer indole reaction.Aromatization of these last compounds with 10 percent palladized charchoal gives 2H,5H-pyridopyrrolopyridin-1-ones providing a new reaction pathway to this series which is more convenient that the one described in the preceding paper.Whereas the alkylation of the N-matallated species derived from 1-chloro-4-methyl-5H-pyridopyrrolopyridine by alkyl halides leads to the mixture of N-5 and N-8 alkyl derivatives, 1-chloro-5H-pyridopyrrolopyridine gives only the N-5 alkylated compound.

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