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1H-Pyrazole, 5-bromo-1-methyl-4-nitro-, also known as 5-bromo-1-methyl-4-nitro-1H-pyrazole, is a chemical compound with the molecular formula C4H4BrN3O2. It is a pyrazole derivative characterized by the presence of a bromine atom at the fifth carbon, a methyl group, and a nitro group attached to the first carbon. 1H-Pyrazole, 5-bromo-1-methyl-4-nitrois widely utilized in organic synthesis and medicinal chemistry research as a building block and intermediate for the synthesis of various pharmaceuticals and agrochemicals. Its unique chemical structure and properties also make it a promising candidate for the development of new drugs and materials. However, due to its potential hazards, it is crucial to handle this chemical with care and adhere to proper safety protocols.

89607-13-6

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89607-13-6 Usage

Uses

Used in Organic Synthesis:
1H-Pyrazole, 5-bromo-1-methyl-4-nitrois used as a building block in organic synthesis for the creation of various chemical compounds. Its unique structure allows for the formation of diverse molecules with potential applications in different fields.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 1H-Pyrazole, 5-bromo-1-methyl-4-nitroserves as an intermediate for the synthesis of pharmaceuticals. Its presence in the molecular structure can contribute to the development of new drugs with improved therapeutic properties.
Used in Pharmaceutical Development:
1H-Pyrazole, 5-bromo-1-methyl-4-nitrois used as a key component in the development of new pharmaceuticals. Its unique chemical properties can enhance the efficacy and safety of medications, leading to better treatment options for various diseases and conditions.
Used in Agrochemicals Synthesis:
1H-Pyrazole, 5-bromo-1-methyl-4-nitrois also utilized in the synthesis of agrochemicals, such as pesticides and herbicides. Its incorporation into these products can improve their effectiveness in controlling pests and weeds, contributing to increased crop yields and agricultural productivity.
Used in Material Science:
Due to its unique chemical structure, 1H-Pyrazole, 5-bromo-1-methyl-4-nitrohas potential applications in the development of new materials with specific properties. These materials can be used in various industries, such as electronics, aerospace, and automotive, to enhance performance and durability.

Check Digit Verification of cas no

The CAS Registry Mumber 89607-13-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,6,0 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 89607-13:
(7*8)+(6*9)+(5*6)+(4*0)+(3*7)+(2*1)+(1*3)=166
166 % 10 = 6
So 89607-13-6 is a valid CAS Registry Number.

89607-13-6SDS

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 5-bromo-1-methyl-4-nitropyrazole

1.2 Other means of identification

Product number -
Other names 1H-Pyrazole,5-bromo-1-methyl-4-nitro

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:89607-13-6 SDS

89607-13-6Relevant academic research and scientific papers

AMINATION OF ISOMERIC BROMO-1-METHYLNITROPYRAZOLES

Perevalov, V. P.,Baryshnenkova, L. I.,Andreeva, M. A.,Manaev, Yu. A.,Denisova, I. A.,et al.

, p. 1322 - 1326 (2007/10/02)

A method was developed for the synthesis of 5-bromo-1-methyl-4-nitropyrazole from 1-methylpyrazole.In the reaction with 25percent aqueous ammonia at 180-190 deg C, 5-bromo-1-methyl-4-nitropyrazole is readily converted to 5-amino-1-methyl-4-nitropyrazole; the production of 4-amino-1-methyl-5-nitropyrazole from 4-bromo-1-methyl-5-nitropyrazole requires the presence of a copper catalyst; under the same conditions in the amination of 4-bromo-1-methyl-3-nitropyrazole, 4-amino-1-methyl-3-nitro- and 1-methyl-3-nitropyrazoles are formed in a 2 : 3 ratio.

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