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1086838-46-1

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1086838-46-1 Usage

Description

5-Bromo-3-nitropyridine-2-carboxylic acid is a chemical compound derived from pyridine, a six-membered heterocyclic compound. It features a bromine and nitro group at specific positions on the pyridine ring, which endows it with unique structural and reactivity properties. 5-Bromo-3-nitropyridine-2... has been studied for its potential pharmaceutical and agricultural applications, particularly as an intermediate in the synthesis of other organic compounds. Its versatility in the creation of new materials and compounds for various purposes, along with its potential use in the development of new chemical processes and technologies, makes 5-Bromo-3-nitropyridine-2-carboxylic acid a valuable compound in the field of chemistry and related industries.

Uses

Used in Pharmaceutical Industry:
5-Bromo-3-nitropyridine-2-carboxylic acid is used as an intermediate in the synthesis of pharmaceutical compounds for various therapeutic applications. Its unique structure and reactivity allow for the development of new drugs with improved efficacy and selectivity.
Used in Agricultural Industry:
In the agricultural sector, 5-Bromo-3-nitropyridine-2-carboxylic acid is used as an intermediate in the synthesis of agrochemicals, such as pesticides and herbicides. Its potential use in this industry contributes to the development of more effective and environmentally friendly solutions for crop protection.
Used in Chemical Research:
5-Bromo-3-nitropyridine-2-carboxylic acid is utilized in chemical research as a valuable compound for studying the properties and reactions of pyridine derivatives. Its unique structure provides insights into the reactivity and behavior of similar compounds, aiding in the advancement of chemical knowledge and the discovery of new materials and processes.
Used in Material Science:
In the field of material science, 5-Bromo-3-nitropyridine-2-carboxylic acid is employed in the development of new materials with specific properties. Its unique structure and reactivity contribute to the creation of innovative materials for various applications, such as sensors, catalysts, and advanced materials for energy storage and conversion.
Used in Chemical Process Development:
5-Bromo-3-nitropyridine-2-carboxylic acid is also used in the development of new chemical processes and technologies. Its potential applications in this area include the improvement of existing processes, the creation of new synthetic routes, and the development of innovative technologies for various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1086838-46-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,6,8,3 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1086838-46:
(9*1)+(8*0)+(7*8)+(6*6)+(5*8)+(4*3)+(3*8)+(2*4)+(1*6)=191
191 % 10 = 1
So 1086838-46-1 is a valid CAS Registry Number.

1086838-46-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Bromo-3-nitropyridine-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 5-bromo-3-nitropyridine-2-carboxaldehyde

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:1086838-46-1 SDS

1086838-46-1Downstream Products

1086838-46-1Relevant articles and documents

ENANTIOMERICALLY ENRICHED ARYLOAZOL-2-YL CYANOETHYLAMINO COMPOUNDS, METHOD OF MAKING AND METHOD OF USING THEREOF

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Page/Page column 88, (2010/06/13)

The present invention relates to novel aryloazol-2-yl-cyanoethylamino derivatives substantially enriched in an enantiomer of formula (I): and compounds of formula (IH) wherein R3, R4, R5, R6, R7, R13a, R13b, R14a, R14b, P, Q, V, W, X, Y, Z and a are as defined in the description, compositions thereof, processes for their preparation and their uses as pesticides.

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