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1-(bromomethyl)-5-ethyl-3-methyl-5-phenylpyrimidine-2,4,6(1H,3H,5H)-trione is a complex chemical compound featuring a pyrimidine ring with various substituents, including a bromomethyl, ethyl, methyl, and phenyl group. As a trione compound, it contains three carbonyl groups, which may contribute to its reactivity and potential applications in various fields. The presence of multiple functional groups suggests that 1-(bromomethyl)-5-ethyl-3-methyl-5-phenylpyrimidine-2,4,6(1H,3H,5H)-trione could have diverse chemical properties, making it a candidate for use in pharmaceuticals, agrochemicals, or materials science. Due to its complex structure and potential reactivity, it is essential to handle 1-(bromomethyl)-5-ethyl-3-methyl-5-phenylpyrimidine-2,4,6(1H,3H,5H)-trione with care and under proper safety conditions.

50441-27-5

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50441-27-5 Usage

Uses

Used in Pharmaceutical Industry:
1-(bromomethyl)-5-ethyl-3-methyl-5-phenylpyrimidine-2,4,6(1H,3H,5H)-trione is used as an intermediate in the synthesis of various pharmaceutical compounds due to its potential reactivity and the presence of multiple functional groups. These groups can be further modified to create new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(bromomethyl)-5-ethyl-3-methyl-5-phenylpyrimidine-2,4,6(1H,3H,5H)-trione is used as a building block for the development of novel agrochemicals, such as pesticides and herbicides. Its complex structure and functional groups can be tailored to target specific pests or weeds, potentially leading to more effective and selective products.
Used in Materials Science:
1-(bromomethyl)-5-ethyl-3-methyl-5-phenylpyrimidine-2,4,6(1H,3H,5H)-trione is used as a component in the development of advanced materials, such as polymers and coatings, due to its potential to form strong intermolecular interactions. Its complex structure and functional groups can contribute to the creation of materials with unique properties, such as enhanced stability, durability, or specific binding capabilities.

Check Digit Verification of cas no

The CAS Registry Mumber 50441-27-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,4,4 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 50441-27:
(7*5)+(6*0)+(5*4)+(4*4)+(3*1)+(2*2)+(1*7)=85
85 % 10 = 5
So 50441-27-5 is a valid CAS Registry Number.

50441-27-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(bromomethyl)-5-ethyl-3-methyl-5-phenyl-1,3-diazinane-2,4,6-trione

1.2 Other means of identification

Product number -
Other names 2,4,6(1H,3H,5H)-Pyrimidinetrione,1-(bromomethyl)-5-ethyl-3-methyl-5-phenyl

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:50441-27-5 SDS

50441-27-5Upstream product

50441-27-5Downstream Products

50441-27-5Relevant academic research and scientific papers

Anticonvulsants. III. Phenobarbital and mephobarbital derivatives

Vida,Hooker,Reinhard

, p. 602 - 605 (1973)

Several phenobarbital and mephobarbital derivatives were found to possess potent anticonvulsant activity and yet were either devoid of the marked hypnotic effects associated with the parent compounds or displayed very weak hypnotic activity. Particularly active compounds were the Mannich type derivatives, the bis(hexamethylenetetramine salt) of 1,3 bis(bromomethyl)phenobarbital and 1 methyl 3 methoxymethylphenobarbital.

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