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5-Bromo-3-nitro-2-(1H-pyrazol-1-yl)pyridine 98% is a pyridine derivative chemical compound with a molecular formula of C8H5BrN4O2. It is characterized by its yellow powder form, a molecular weight of 261.05 g/mol, and a high purity level of 98%. 5-Bromo-3-nitro-2-(1H-pyrazol-1-yl)pyridine 98% features bromine, nitro, and pyrazole functional groups, which contribute to its high reactivity and versatile nature in forming diverse chemical bonds. It is widely recognized as a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds, making it a staple in research and industrial applications.

446284-40-8

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446284-40-8 Usage

Uses

Used in Pharmaceutical Industry:
5-Bromo-3-nitro-2-(1H-pyrazol-1-yl)pyridine 98% is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to form complex molecular structures. Its presence in drug development aids in creating novel therapeutic agents with potential applications in treating a range of diseases.
Used in Agrochemical Industry:
In the agrochemical sector, 5-Bromo-3-nitro-2-(1H-pyrazol-1-yl)pyridine 98% is utilized as a building block for the development of new pesticides and herbicides. Its reactivity and functional groups allow for the creation of compounds that can effectively control pests and weeds, thereby enhancing crop protection.
Used in Organic Synthesis Research:
5-Bromo-3-nitro-2-(1H-pyrazol-1-yl)pyridine 98% is employed as a research compound in organic synthesis, where its high reactivity and functional groups are leveraged to explore new chemical reactions and pathways. This contributes to the advancement of organic chemistry and the discovery of new synthetic methods.
Used in Chemical Intermediates Production:
As a chemical intermediate, 5-Bromo-3-nitro-2-(1H-pyrazol-1-yl)pyridine 98% is used in the production of other organic compounds. Its role in this capacity is crucial for the synthesis of a variety of specialty chemicals used across different industries.
Used in Material Science:
In the field of material science, 5-Bromo-3-nitro-2-(1H-pyrazol-1-yl)pyridine 98% is utilized in the development of new materials with unique properties. Its incorporation into material formulations can lead to the creation of substances with enhanced characteristics, such as improved stability or reactivity, for specific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 446284-40-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,6,2,8 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 446284-40:
(8*4)+(7*4)+(6*6)+(5*2)+(4*8)+(3*4)+(2*4)+(1*0)=158
158 % 10 = 8
So 446284-40-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H5BrN4O2/c9-6-4-7(13(14)15)8(10-5-6)12-3-1-2-11-12/h1-5H

446284-40-8SDS

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-3-nitro-2-(1H-pyrazol-1-yl)pyridine

1.2 Other means of identification

Product number -
Other names 5-bromo-3-nitro-2-pyrazol-1-ylpyridine

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:446284-40-8 SDS

446284-40-8Downstream Products

446284-40-8Relevant academic research and scientific papers

Composition and antiviral activity of substituted azaindoleoxoacetic piperazine derivatives

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Page 78-79, (2008/06/13)

This invention provides compounds having drug and bio-affecting properties, their pharmaceutical compositions and method of use. In particular, the invention is concerned with azaindoleoxoacetyl piperazine derivatives. These compounds possess unique antiviral activity, whether used alone or in combination with other antivirals, antiinfectives, immunomodulators or HIV entry inhibitors. More particularly, the present invention relates to the treatment of HIV and AIDS.

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