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4-Bromo-2-methylpyrimidine is a pyrimidine derivative with the molecular formula C5H5BrN2, featuring a bromine atom and a methyl group attached to the pyrimidine ring. It is a chemical compound that serves as a versatile building block in the synthesis of pharmaceuticals and agrochemicals, as well as an intermediate in the production of other organic compounds. With its potential applications in medicinal chemistry, 4-Bromo-2-methylpyrimidine is under active research for its biological activity and therapeutic uses. However, it is crucial to handle 4-Bromo-2-methylpyrimidine with care due to its potential health hazards and harmful effects if not used properly.

1114560-76-7

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1114560-76-7 Usage

Uses

Used in Pharmaceutical Industry:
4-Bromo-2-methylpyrimidine is used as a building block for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique chemical structure allows for the creation of diverse compounds with potential medicinal properties.
Used in Agrochemical Industry:
In the agrochemical industry, 4-Bromo-2-methylpyrimidine is utilized as a building block in the synthesis of agrochemicals, such as pesticides and herbicides. Its incorporation into these compounds can enhance their effectiveness in controlling pests and weeds, thereby improving crop yields and quality.
Used in Organic Chemistry Research:
4-Bromo-2-methylpyrimidine serves as an intermediate in the production of other organic compounds, playing a crucial role in organic chemistry research. Its versatile structure allows for further functionalization and modification, enabling the synthesis of a wide range of organic molecules with various applications.
Used in Medicinal Chemistry:
4-Bromo-2-methylpyrimidine is actively researched for its potential applications in medicinal chemistry. Its unique structure and properties make it a promising candidate for the development of new drugs and therapeutic agents, particularly in the areas of antiviral, anticancer, and antimicrobial treatments.
Safety Precautions:
Due to the potential health hazards and harmful effects of 4-Bromo-2-methylpyrimidine, it is essential to handle 4-Bromo-2-methylpyrimidine with caution. Proper safety measures, such as wearing protective clothing, using gloves and eye protection, and working in a well-ventilated area, should be taken to minimize the risk of exposure. Additionally, it is crucial to follow the recommended guidelines and regulations for the storage, handling, and disposal of this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 1114560-76-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,4,5,6 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1114560-76:
(9*1)+(8*1)+(7*1)+(6*4)+(5*5)+(4*6)+(3*0)+(2*7)+(1*6)=117
117 % 10 = 7
So 1114560-76-7 is a valid CAS Registry Number.

1114560-76-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Bromo-2-methylpyrimidine

1.2 Other means of identification

Product number -
Other names 4-bromo-2-methyl-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:1114560-76-7 SDS

1114560-76-7Upstream product

1114560-76-7Downstream Products

1114560-76-7Relevant academic research and scientific papers

A method for preparing 2, 4 - substituted pyrimidine

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Paragraph 0010; 0018-0019, (2019/06/05)

The invention belongs to the technical field of the synthesized compounds, in particular to a 2, 4 - substituted pyrimidine of the preparation method. The method comprises the following steps: 1) the 2 - substituted pyrimidine dissolved in tetrahydrofuran, in - 60 — - 78 °C lower dropping TMP.MgCl.LiCl, dropping 1 h after adding anhydrous zinc chloride, raising the temperature to room temperature, dropping halogen, 2 h after adding hydrochloric acid solution quenching reaction; 2) reaction of the reaction solution in order to ethyl acetate extraction, drying of the organic layer concentrated, column chromatography purification to obtain the product. The invention compared with the prior art, in order to 2 - substituted pyrimidines as raw materials can be specific selection 4 substituted, at the same time does not produce 5 substituted by-product, with good selectivity, single product, is easy to be purified, with mild reaction conditions, the reaction speed and the like.

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