13500-24-8

Usage

Uses

Used in Organic Synthesis:
5-(4'-METHOXYBENZYL)-5-METHYLHYDANTOIN is used as a key intermediate in the synthesis of various organic compounds. Its chemical structure allows it to be a versatile building block for the development of new molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-(4'-METHOXYBENZYL)-5-METHYLHYDANTOIN is used as a starting material for the development of new drugs. Its unique chemical properties enable the creation of novel drug candidates with potential therapeutic benefits.
Used in Chemical Research:
5-(4'-METHOXYBENZYL)-5-METHYLHYDANTOIN is also used in chemical research as a model compound to study various reaction mechanisms and to develop new synthetic methodologies. This helps researchers gain a deeper understanding of chemical processes and contributes to the advancement of the field.
Used in Material Science:
In the field of material science, 5-(4'-METHOXYBENZYL)-5-METHYLHYDANTOIN can be used as a component in the development of new materials with specific properties. Its unique chemical structure can contribute to the creation of materials with improved performance in various applications.
Used in Agrochemical Industry:
5-(4'-METHOXYBENZYL)-5-METHYLHYDANTOIN is also utilized in the agrochemical industry as a starting material for the synthesis of new pesticides or other agrochemical products. Its chemical properties make it a valuable component in the development of innovative solutions for agricultural challenges.

Upstream product

• 122-84-9 4-methoxybenzyl methyl ketone 
• 151-50-8 potassium cyanide 
• 506-87-6 ammonium carbonate 

Downstream Products

• 13500-25-9 5-(4-hydroxy-benzyl)-5-methyl-imidazolidine-2,4-dione 
• 113806-23-8 N-3-(2'-hydroxypropyl)-5-p.methoxylbenzyl-5-methylhydantoin 
• 113806-23-8 N-3-(2'-hydroxypropyl)-5-p.methoxylbenzyl-5-methylhydantoin 
• 7373-63-9 4-Hydroxy-3,5-diiod-α-methyl-phenyl-alanin-aethylester 
• 7434-77-7 2-amino-3-(4-hydroxy-3,5-diiodo-phenyl)-2-methyl-propionic acid 
• 658-48-0 2-amino-3-(4-hydroxy-phenyl)-2-methyl-propionic acid 
• 5487-34-3 5-[4-(4-methoxy-phenoxy)-3,5-dinitro-benzyl]-5-methyl-imidazolidine-2,4-dione 
• 13500-38-4 5-(4-hydroxy-3,5-dinitro-benzyl)-5-methyl-imidazolidine-2,4-dione 
• 95525-89-6 N²-<(S)-N²-acetyl-2,O⁴-dimethyltyrosyl>-L-phenylalanine dimethylamide 
• 95525-90-9 N²-<(R)-N²-acetyl-2,O⁴-dimethyltyrosyl>-L-phenylalanine dimethylamide 
• 96574-52-6 (R)-N²-acetyl-2,O⁴-dimethyltyrosine 
• 96574-31-1 N²-acetyl-2,O⁴-dimethyltyrosine 
• 96574-51-5 (S)-N²-acetyl-2,O⁴-dimethyltyrosine 
• 7383-30-4 2-amino-3-(4-methoxyphenyl)-2-methylpropionic acid 

Relevant academic research and scientific papers

SIMPLE PREPARATIONS OF SOME HYDANTOINS OF PHENYLALANINE AND α-MePhe AND THEIR CHIRAL STABILITY DURING N3-ALKYLATION. A ROUTE TO THE SYNTHESIS OF CHIRAL AMINES

Preparations of chiral-pure hydantoins derived from L-Phe and L-α-MePhe are revisited.A one step quantitative route for 5-benzyl-5-methyl hydantoin is obtained by melting α-MePhe with ureum.L-Phe-hydantoin could not be alkylated at N-3 with conservation of chirality at C-5.Diastereomers resulting from asymmetric alkyl groupings implanted at N-3 can be separated by crystallization in aqueous medium.The N-3 alkylated hydantoins can be hydrolyzed in high yields with Ba(OH)2.This allows the preparation of enantiomeric pure amines such like 2-methylbutylamine and 2-hydroxypropylamine via N-3 alkylation of the chirally-stable hydantoin of α-MePhe followed by enantiomeric resolution and hydrolysis.