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2-Amino-4-bromo-3-nitropyridine is a chemical compound characterized by the molecular formula C5H4BrN3O2. It is a yellow crystalline solid that serves as an intermediate in the synthesis of pharmaceuticals and agrochemicals. This nitro-substituted pyridine derivative features an amino group, a bromine atom, and a nitro group attached to the pyridine ring. Due to its potential mutagenic and carcinogenic properties, the use and handling of 2-Amino-4-bromo-3-nitropyridine must adhere to proper safety protocols and regulations.

84487-10-5

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84487-10-5 Usage

Uses

Used in Pharmaceutical Industry:
2-Amino-4-bromo-3-nitropyridine is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Amino-4-bromo-3-nitropyridine is utilized as a precursor in the production of pesticides and other agrochemicals. Its chemical properties enable the creation of effective solutions for pest control and crop protection.

Check Digit Verification of cas no

The CAS Registry Mumber 84487-10-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,4,8 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 84487-10:
(7*8)+(6*4)+(5*4)+(4*8)+(3*7)+(2*1)+(1*0)=155
155 % 10 = 5
So 84487-10-5 is a valid CAS Registry Number.

84487-10-5SDS

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 2-Amino-4-bromo-3-nitropyridine

1.2 Other means of identification

Product number -
Other names 4-bromo-3-nitropyridin-2-amine

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:84487-10-5 SDS

84487-10-5Relevant academic research and scientific papers

A model D - amino acid oxidase inhibitor and its preparation and application

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Paragraph 0307; 0309, (2019/02/02)

The invention provides a novel D- amino acid oxidase inhibitor and a preparation and application thereof. In particular, the invention discloses derivatives of quinoxaline-2,3-diketone, which has a novel structure shown in formula A, as well as a preparation method thereof and an application as an inhibitor of D-amino acid oxidase (DAAO). The compound provided by the invention shows excellent effects of analgesia and blocking morphine analgesia tolerance, and has application value for analgesia, treating opiate drug tolerance, and anti-schizophrenia.

Kinetic Studies of the Mechanism of the Nitraminopyridine Rearrangement

Deady, Leslie W.,Korytsky, Olga L.

, p. 2035 - 2040 (2007/10/02)

Rate data are reported for the rearrangement, in 92percent sulfuric acid at 30 deg C, of a series of 4-X-2-nitraminopyridines (X=H, Me, Br, Cl, MeO, CO2H) and of 4-methyl-2-nitramino(3-D)-pyridine.Values of pKa for second protonation of the corresponding pyridin-2-amines were also measured and rate constants for nitration of the monoprotonated pyridinamines were thereby calculated.The results suggest that the rate-determining step occurs prior to formation of the appropriate 3- and 5-nitro ? complexes.The nature of this step is not clear, however, and a key role for the nitramine itself is not proven by the current evidence

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