89417-94-7

Usage

Uses

Used in Medicinal Chemistry:
(4-Thioxo-[1,3,5]triazinan-1-yl)-acetic acid is used as a building block for the development of new pharmaceutical compounds due to its unique chemical structure and potential biological activity.
Used in Drug Design:
(4-THIOXO-[1,3,5]TRIAZINAN-1-YL)-ACETIC ACID is utilized as a key component in the design of novel drugs, particularly those targeting viral and tumor-related diseases, thanks to its potential antiviral and antitumor properties.
Used in Antiviral Applications:
(4-Thioxo-[1,3,5]triazinan-1-yl)-acetic acid is being studied for its potential as an antiviral agent, which could be used to combat various viral infections.
Used in Antitumor Applications:
(4-THIOXO-[1,3,5]TRIAZINAN-1-YL)-ACETIC ACID is also being investigated for its potential as an antitumor agent, which could be employed in the development of cancer treatments.
Used in Herbicide Development:
(4-Thioxo-[1,3,5]triazinan-1-yl)-acetic acid is being explored for its potential use in the development of new herbicides, which could be employed in agriculture to control unwanted plant growth.
Used in Organic Synthesis:
This chemical is used as a versatile building block in the synthesis of various organic compounds, contributing to the advancement of chemical research and the development of new materials and products.

Upstream product

• 50-00-0 formaldehyd 
• 17356-08-0 thiourea 
• 56-40-6 glycine 

Relevant academic research and scientific papers

NEW ANTIBACTERIAL PRODUCTS

The invention provides novel antibacterial compounds of formulae IA, IB and IC as defined herein. Optionally, the antibacterial compounds can be bonded to a delivery agent that is capable of bonding to one or more structures on a bacterial cell membrane. The invention also provides the use of such compounds in treating or preventing bacterial infections, and processes for their synthesis.

Alkylation of cyclic Mannich bases, derivatives of thiourea and simple amino acids

Aminomethylation of thiourea with aqueous formaldehyde and simple amino acids (glycine, β-alanine, γ-aminobutyric acid) have resulted in the formation of (4-thioxo-1,3,5-triazinan-1-yl)-substituted acetic, propionic, and butyric acids, respectively. By alkylation of these compounds corresponding S-methyl and S-ethyl iodides were obtained, and by the action of tert-butylamine, the corresponding salts. The same salts were obtained by the reaction of amine exchange between 5-tert-butyl-1,3,5-triazinan-2-thione and these amino acids in water. As a result of neutralization of S-methyl iodides with tert-butylamine in 2-propanol or aqueous 2-propanol zwitterionic [4-(methyl-sulfanyl)-3,6-dihydro-1,3,5-triazin-1(2H)-yl] derivatives of these acids were isolated. From aqueous solutions of S-methyl iodides and tert-butylamine ion associates of the corresponding zwitter-ions and tert-butylammonium iodide have crystallized. The same associates have formed at treating S-methyl iodides with tert-butylamine or diethylamine in the absence of a solvent. Pleiades Publishing, Ltd., 2012.