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.
50441-27-5Relevant articles and documents
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.
