3366-93-6

Usage

Uses

Used in Pharmaceutical Industry:
1-ALLYLHYDANTOIN is used as a key intermediate for the production of pharmaceuticals, playing a significant role in the synthesis of various medicinal compounds due to its reactive chemical structure.
Used in Agrochemical Industry:
In the agrochemical sector, 1-ALLYLHYDANTOIN is utilized as an intermediate in the synthesis of agrochemicals, contributing to the development of products designed to enhance crop protection and yield.
Used in Specialty Chemicals Production:
1-ALLYLHYDANTOIN serves as an intermediate in the manufacturing process of specialty chemicals, which are tailored for specific applications and often exhibit unique properties not found in commodity chemicals.
Used in Polymer Synthesis:
1-ALLYLHYDANTOIN is used as a building block in the synthesis of polymers, which are large molecules composed of repeating structural units, and are essential in a wide array of industries, including plastics, textiles, and coatings.
Used as a Stabilizer for Hydrogen Peroxide:
1-ALLYLHYDANTOIN is employed as a stabilizer in hydrogen peroxide solutions, helping to prevent decomposition and maintain the stability and effectiveness of the hydrogen peroxide for various applications.
Used in Materials Science:
1-ALLYLHYDANTOIN has been studied for its potential applications in materials science, where it may contribute to the development of new materials with enhanced properties for specialized uses.
Used as a Chelating Agent in Metal Ion Extraction:
This versatile compound is also used as a chelating agent for the extraction of metal ions, a process that is important in various industrial applications, including wastewater treatment and metal recovery.

Upstream product

• 1345028-64-9 C₇H₁₀N₂O₂ 

Downstream Products

• 204072-96-8 (2R,4S)-4-(3-Allyl-2,5-dioxo-imidazolidin-1-yl)-1-(4-butoxy-benzenesulfonyl)-pyrrolidine-2-carboxylic acid methyl ester 
• 1053615-65-8 (2R,4S)-4-(3-Allyl-2,5-dioxo-imidazolidin-1-yl)-1-(4-propoxy-benzenesulfonyl)-pyrrolidine-2-carboxylic acid methyl ester 

Relevant academic research and scientific papers

HYDANTOIN CONTAINING DEOXYURIDINE TRIPHOSPHATASE INHIBITORS

Provided herein are dUTPase inhibitors, compositions comprising such compounds and methods of using such compounds and compositions.

HYDANTOIN CONTAINING DEOXYURIDINE TRIPHOSPHATASE INHIBITORS

Provided herein are dUTPase inhibitors, compositions comprising such compounds and methods of using such compounds and compositions.

AMINO SULFONYL COMPOUNDS

Provided herein are dUTPase inhibitors, compositions comprising such compounds and methods of using such compounds and compositions.

NITROGEN RING LINKED DEOXYURIDINE TRIPHOSPHATASE INHIBITORS

Provided herein are dUTPase inhibitors, compositions comprising such compounds and methods of using such compounds and compositions.

6-MEMBERED URACIL ISOSTERES

Provided herein are dUTPase inhibitors, compositions comprising such compounds and methods of using such compounds and compositions.

URACIL CONTAINING COMPOUNDS

Provided herein are dUTPase inhibitors, compositions comprising such compounds and methods of using such compounds and compositions.

HYDANTOIN CONTAINING DEOXYURIDINE TRIPHOSPHATASE INHIBITORS

Provided herein are dUTPase inhibitors, compositions comprising such compounds and methods of using such compounds and compositions.

DEOXYURIDINE TRIPHOSPHATASE INHIBITORS CONTAINING AMINO SULFONYL LINKAGE

Provided herein are dUTPase inhibitors, compositions comprising such compounds and methods of using such compounds and compositions.

Highly efficient dialkylphosphate-mediated syntheses of hydantoins and a bicyclohydantoin under solvent-free conditions

Diversely substituted hydantoins have been synthesized by new strategy from cyanamide based precursor, that is, methyl N-cyano-N-alkyl/arylaminoacetate. Dialkylphosphates were employed as the mild reagent to hydrolyze and cyclize the substrate in one step to give quantitative yields of the desired products. Syntheses of multivalent hydantoins viz bis-hydantoin, bicyclohydantoin have potentially widened the scope and applicability of the present method. Solvent-free conditions and very easy work-up procedure make the reaction convenient and eco-friendly. Single crystal structures of some of the representative compounds are also reported.

PROCESS FOR STRAIGHTENING KERATIN FIBRES WITH A HEATING MEANS AND DENATURING AGENTS

The invention relates to a process for straightening keratin fibres, comprising: (i) a step in which a straightening composition containing at least two denaturing agents is applied to the keratin fibres, (ii) a step in which the temperature of the keratin fibres is raised, using a heating means, to a temperature of between 110 and 250° C.