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3-Amino-5-chloropicoline, a pyridine derivative with the molecular formula C6H6ClN3, is a chemical compound that features an amino group and a chlorine atom. It is recognized for its moderate toxicity and is a significant contributor to the synthesis of pharmaceuticals and agrochemicals, as well as a candidate for catalytic applications in organic reactions. Its unique properties and potential uses render it a valuable asset in the realm of chemical research and development.

89639-36-1

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89639-36-1 Usage

Uses

Used in Pharmaceutical Synthesis:
3-Amino-5-chloropicoline is utilized as a key intermediate in the production of various pharmaceuticals. Its presence in the molecular structure allows for the development of new drugs with specific therapeutic properties, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Production:
In the agrochemical industry, 3-Amino-5-chloropicoline serves as a building block for the creation of pesticides and other crop protection agents. Its incorporation into these compounds can enhance their effectiveness in protecting crops from pests and diseases, thereby supporting agricultural productivity.
Used as a Catalyst in Organic Reactions:
3-Amino-5-chloropicoline has been studied for its potential as a catalyst in various organic reactions. Its unique chemical properties enable it to facilitate and accelerate chemical processes, making it a promising candidate for improving the efficiency and selectivity of synthetic pathways in organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 89639-36-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,6,3 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 89639-36:
(7*8)+(6*9)+(5*6)+(4*3)+(3*9)+(2*3)+(1*6)=191
191 % 10 = 1
So 89639-36-1 is a valid CAS Registry Number.

89639-36-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Chloro-2-methylpyridin-3-amine

1.2 Other means of identification

Product number -
Other names 5-chloro-2-methylpyridin-3-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:89639-36-1 SDS

89639-36-1Relevant academic research and scientific papers

AZAINDOLE CARBOXAMIDE COMPOUNDS FOR THE TREATMENT OF MYCOBACTERIAL INFECTIONS

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Page/Page column 172-173, (2021/04/02)

Provided herein are compounds of Formula (I) and Formula (II): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of tuberculosis.

(PYRIDIN-2-YL)AMINE DERIVATIVES AS TGF-BETA R1 (ALK5) INHIBITORS FOR THE TREATMENT OF CANCER

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Paragraph 00273, (2020/07/15)

The present invention relates to pharmaceutical compounds, compositions and methods, especially as they are related to compositions and methods for the treatment and/or prevention of a proliferation disorder associated with ΤGFβR1 activity, such as a cancer or fibrosis. The invention provides compounds of Formula (I) and Formula (II) as further described herein having an acidic moiety that enhances tissue specificity for targeted tissues and organs. The invention includes pharmaceutical compositions, pharmaceutical combinations, and methods of use of these compounds for treating conditions including cancer or fibrosis.

NOVEL COMPOUNDS AS WIP1 INHIBITORS

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Page/Page column 48, (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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