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5-Bromo-1-methyl-1H-pyrazole-4-carbonitrile is a chemical compound characterized by the molecular formula C5H4BrN3. It is a nitrile derivative of the pyrazole ring, featuring a bromine atom and a methyl group attached to the pyrazole structure. 5-Bromo-1-methyl-1H-pyrazole-4-carbonitrile serves as a versatile intermediate in the synthesis of a variety of organic compounds, particularly in the pharmaceutical and agrochemical industries, due to its potential biological activities and its role as a building block for the creation of biologically active molecules.

1269293-80-2

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1269293-80-2 Usage

Uses

Used in Organic Synthesis:
5-Bromo-1-methyl-1H-pyrazole-4-carbonitrile is utilized as a reagent in organic synthesis for the preparation of a range of pharmaceuticals and agrochemicals. Its unique structure allows for the development of new compounds with potential therapeutic and pesticidal properties.
Used in Drug Discovery and Development:
As a valuable intermediate, 5-Bromo-1-methyl-1H-pyrazole-4-carbonitrile is employed in drug discovery and development processes. Its potential biological activities, such as enzyme inhibition, make it a promising candidate for the creation of new drugs targeting specific biological pathways.
Used in Enzyme Inhibition Studies:
5-Bromo-1-methyl-1H-pyrazole-4-carbonitrile has been studied for its potential as an inhibitor of certain enzymes. This application is crucial in the development of drugs that can modulate enzyme activity, thereby affecting various biological processes and treating diseases.
Used in the Synthesis of Biologically Active Molecules:
5-Bromo-1-methyl-1H-pyrazole-4-carbonitrile also serves as a building block for the synthesis of biologically active molecules. Its structural features make it a key component in the creation of new molecules with potential applications in medicine and agriculture, contributing to the advancement of novel therapeutic agents and crop protection products.

Check Digit Verification of cas no

The CAS Registry Mumber 1269293-80-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,9,2,9 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1269293-80:
(9*1)+(8*2)+(7*6)+(6*9)+(5*2)+(4*9)+(3*3)+(2*8)+(1*0)=192
192 % 10 = 2
So 1269293-80-2 is a valid CAS Registry Number.

1269293-80-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-bromo-1-methylpyrazole-4-carbonitrile

1.2 Other means of identification

Product number -
Other names 5-BROMO-1-METHYL-1H-PYRAZOLE-4-CARBONITRILE

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:1269293-80-2 SDS

1269293-80-2Downstream Products

1269293-80-2Relevant academic research and scientific papers

PROCESS OF PREPARATION OF AZIMSULFURON

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Paragraph 0229, (2015/04/28)

The present disclosure provides process for preparation of azimsulfuron or its salts, isomers, and other derivatives thereof. The process involves treating a compound of formula I, with aqueous acetic acid or formic acid and chlorine gas or sodium hypochlorite in presence of hydrochloric acid in chlorinated solvents such as dichloromethane, 1,2-dichloroethane or with aqueous acetic acid and N-chlorosuccinimide or hydrogen peroxide in presence of hydrochloric acid in aqueous cyclic ether such as tetrahydrofuran, 1,4-dioxane to obtain 1-methyl-4-(2-methyl-2H-tetrazol-5-yl)-1H-pyrazole-5-sulfonyl chloride; converting the sulfonyl chloride to a sulfonamide and treating the sulfonamide with a phenyl(4,6-dimethoxypyrimidin-2-yl) carbamate to obtain azimsulfuron or its salts, isomers, and other derivatives thereof.

PROCESS OF PREPARATION OF AZIMSULFURON

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Page/Page column 41, (2014/01/17)

The present disclosure provides process for preparation of azimsulfuron or its salts, isomers, and other derivatives thereof. The process involves treating a compound of formula I, (Formula I should be inserted here.) with aqueous acetic acid or formic acid and chlorine gas or sodium hypochlorite in presence of hydrochloric acid in chlorinated solvents such as dichloromethane, 1,2-dichloroethane or with aqueous acetic acid and N-chlorosuccinimide or hydrogen peroxide in presence of hydrochloric acid in aqueous cyclic ether such as tetrahydrofuran, 1,4-dioxane to obtain 1-methyl-4-(2-methyl-2H-tetrazol-5-yl)-1H-pyrazole-5-sulfonyl chloride; converting the sulfonyl chloride to a sulfonamide and treating the sulfonamide with a phenyl(4,6-dimethoxypyrimidin-2-yl) carbamate to obtain azimsulfuron or its salts, isomers, and other derivatives thereof.

SUBSTITUTED TETRAZOLE COMPOUNDS AND PROCESS THEREOF

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Page/Page column 100, (2014/01/17)

The present disclosure provides a compound of formula I, its derivatives, salts, stereo-isomers, or regio-isomers thereof, useful as intermediates in preparation of sulfonamide or sulfonyl urea growth regulators or herbicides. Formula I The present disclosure further provides a process for preparing compound of formula I, its derivatives, salts, stereo-isomers, or regio-isomers thereof.

SUBSTITUTUED PYRAZOLE COMPOUNDS AND PROCESS FOR PREPARATION THEREOF.

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Page/Page column 80; 81, (2014/01/17)

The present disclosure provides a compound of formula I, its derivatives, salts, stereo-isomers, or regio-isomers thereof, useful as intermediates in preparation of sulfonamide or sulfonyl urea growth regulators or herbicides. Formula I The present disclosure further provides a process for preparing compound of formula I, its derivatives, salts, stereo-isomers, or regio-isomers thereof.

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