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5-Chloro-2-methyl-3-nitropyridine is a chemical compound characterized by the molecular formula C6H5ClN2O2. It is a yellow crystalline solid with a molecular weight of 172.57 g/mol. 5-Chloro-2-methyl-3-nitropyridine is notable for its presence of a nitro group and a chlorine atom, which contribute to its versatility as a building block in the synthesis of various organic compounds. Due to its potential hazardous nature, it is crucial to handle 5-Chloro-2-methyl-3-nitropyridine with care.

1211533-93-5

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1211533-93-5 Usage

Uses

Used in Pharmaceutical Synthesis:
5-Chloro-2-methyl-3-nitropyridine is utilized as an intermediate in the synthesis of pharmaceuticals, playing a crucial role in the development of new drugs. Its unique structure allows for the creation of a wide range of medicinal compounds.
Used in Agrochemical Production:
In the agrochemical industry, 5-Chloro-2-methyl-3-nitropyridine serves as an intermediate, contributing to the formulation of various agricultural chemicals that help protect crops and enhance their growth.
Used in Dye and Pigment Manufacturing:
5-Chloro-2-methyl-3-nitropyridine is also employed in the production of dyes and pigments, where its chemical properties are leveraged to create a diverse array of colorants for various applications.
Used in Organic Synthesis:
As a versatile building block, 5-Chloro-2-methyl-3-nitropyridine is used in organic synthesis for the preparation of different organic compounds, showcasing its broad applicability in chemical research and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 1211533-93-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,1,5,3 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1211533-93:
(9*1)+(8*2)+(7*1)+(6*1)+(5*5)+(4*3)+(3*3)+(2*9)+(1*3)=105
105 % 10 = 5
So 1211533-93-5 is a valid CAS Registry Number.

1211533-93-5SDS

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 5-Chloro-2-Methyl-3-Nitropyridine

1.2 Other means of identification

Product number -
Other names 5-Chloro-2-methyl-3-nitropyridine

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:1211533-93-5 SDS

1211533-93-5Relevant academic research and scientific papers

3-OXAZOLINONE COMPOUND, PREPARATION METHOD THEREFOR AND PHARMACEUTICAL APPLICATION THEREOF

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Paragraph 0061; 0120; 0122, (2021/04/16)

The present invention relates to a novel 3-indazolinone compound that regulates or inhibits the activity of indoleamine 2,3-dioxygenase (IDO), the method for the preparation thereof and the use thereof in medicine. In particular, the present invention relates to a compound represented by the general formula (I) and a pharmaceutically acceptable salt thereof, a pharmaceutical composition comprising the compound or a pharmaceutically acceptable salt thereof, a method for treating or preventing IDO-mediated diseases, especially tumors, by use of the compound or a pharmaceutically acceptable salt thereof, and a method for preparing the compound or a pharmaceutically acceptable salt thereof. The present invention further relates to use of the compound or a pharmaceutically acceptable salt thereof or a composition comprising the compound or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for treating or preventing IDO-mediated diseases, especially tumors.Wherein the substituents of the general formula (I) are defined the same as that in the specification.

NOVEL COMPOUNDS AS WIP1 INHIBITORS

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Page/Page column 47, (2012/11/13)

This invention relates to the use of acylated alanine derivatives for the modulation, notably the inhibition of the activity of WIP1. Suitably, the present invention relates to the use of acylated alanine derivatives in the treatment of cancer.

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