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2-(6-Bromo-pyridin-3-yl)pyrimidine is a pyrimidine derivative with the molecular formula C10H7BrN4, featuring a bromo-pyridine group attached to the 3-position. This chemical compound is often utilized in medicinal and pharmaceutical research due to its potential applications in the development of new drugs and therapies. Its unique structure allows it to be a valuable building block in organic synthesis for the preparation of various other compounds. Furthermore, it has been studied for its potential biological activities and interactions with proteins, making it a significant tool in biochemical research.

942189-65-3

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942189-65-3 Usage

Uses

Used in Pharmaceutical Research:
2-(6-Bromo-pyridin-3-yl)pyrimidine is used as a chemical intermediate for the development of new drugs and therapies, leveraging its unique structure and potential biological activities.
Used in Organic Synthesis:
In the field of organic synthesis, 2-(6-Bromo-pyridin-3-yl)pyrimidine serves as a building block for the preparation of various other compounds, contributing to the creation of diverse chemical entities.
Used in Biochemical Research:
2-(6-Bromo-pyridin-3-yl)pyrimidine is employed as a valuable tool in biochemical research, where it is studied for its interactions with proteins and potential biological activities, aiding in the understanding of molecular mechanisms and the discovery of novel therapeutic targets.

Check Digit Verification of cas no

The CAS Registry Mumber 942189-65-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,2,1,8 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 942189-65:
(8*9)+(7*4)+(6*2)+(5*1)+(4*8)+(3*9)+(2*6)+(1*5)=193
193 % 10 = 3
So 942189-65-3 is a valid CAS Registry Number.

942189-65-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(6-Bromopyridin-3-yl)pyrimidine

1.2 Other means of identification

Product number -
Other names 2-(6-bromo-pyridin-3-yl)-pyrimidine

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:942189-65-3 SDS

942189-65-3Downstream Products

942189-65-3Relevant academic research and scientific papers

HETEROCYCLIC COMPOUNDS AND USE THEREOF AS ERK INHIBITORS

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Page/Page column 210-211, (2009/01/23)

Disclosed are the ERK inhibitors of formula 1.0: [Formula (1.0)] and the pharmaceutically acceptable salts, esters and solvates thereof. Q is a piperidine or piperazine ring that can have a bridge or a fused ring. The piperidine ring can have a double bond in the ring. All other substitutents are as defined herein. Also disclosed are methods of treating cancer using the compounds of formula 1.0.

POLYCYCLIC INDAZOLE DERIVATIVES THAT ARE ERK INHIBITORS

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Page/Page column 226, (2008/06/13)

Disclosed are the ERK inhibitors of formula 1.0 and the pharmaceutically acceptable salts and solvates thereof. Q is a piperidine or piperazine ring that can have a bridge or a fused ring. The piperidine ring can have a double bond in the ring. All other substitutents are as defined herein. Also disclosed are methods of treating cancer using the compounds of formula 1.0.

PYRROLIDINE DERIVATIVES AS ERK INHIBITORS

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Page/Page column 183, (2010/11/28)

Disclosed are the ERK inhibitors of Formula (1.0): and the pharmaceutically acceptable salts and solvates thereof. Q is a piperidine or piperazine ring that can have a bridge or a fused ring. The piperidine ring can have a double bond in the ring. All other substitutents are as defined herein. Also disclosed are methods of treating cancer using the compounds of Formula (1.0).

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