15998-93-3

Basic information

• Product Name: 5,5-dimethyl-2-thioxoimidazolidin-4-one
• CAS NO: 15998-93-3
• Molecular Formula: C₅H₈N₂OS
• Molecular Weight: 144.1948
• Mol File: 15998-93-3.mol
• Article Data: 5

Chemical Properties

• Density: 1.29g/cm³
• Refractive Index: 1.593
• CAS DataBase Reference: 5,5-dimethyl-2-thioxoimidazolidin-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 5,5-dimethyl-2-thioxoimidazolidin-4-one(15998-93-3)
• EPA Substance Registry System: 5,5-dimethyl-2-thioxoimidazolidin-4-one(15998-93-3)

Safety Data

• Hazardous Substances Data: 15998-93-3(Hazardous Substances Data)

Usage

General Description

5,5-dimethyl-2-thioxoimidazolidin-4-one is a chemical compound with the molecular formula C6H10N2OS. It is a heterocyclic compound that contains a sulfur and nitrogen atom in the five-membered ring structure. 5,5-dimethyl-2-thioxoimidazolidin-4-one is used in medicinal chemistry as a precursor for the synthesis of other organic compounds. It has also been studied for its potential biological activities and pharmacological properties. The structural features of 5,5-dimethyl-2-thioxoimidazolidin-4-one make it a versatile building block for the synthesis of various pharmaceuticals and agrochemicals. Its unique structure and reactivity make it a valuable compound in the field of organic chemistry and drug discovery.

Upstream product

• 20513-25-1 5,5-dimethylimidazolidine-2,4-dithione 
• 62-57-7 2-Aminoisobutyric acid 
• 556-61-6 methyl thioisocyanate 
• 22421-97-2 methyl 2-chloroisobutyrate 
• 17356-08-0 thiourea 
• 61796-07-4 4-(dimethylamino)-5,5-dimethyl-3-imidazolin-2-thione 
• 38451-03-5 1-acetyl-5,5-dimethyl-2-thioxo-imidazolidin-4-one 
• 61796-28-9 4-amino-5,5-dimethyl-1,5-dihydro-imidazole-2-thione 

Downstream Products

• 143782-28-9 2-(trifluoromethyl)-4-(4,4-dimethyl 5-oxo-2-thioimidazolin-1-yl)benzonitrile 

Relevant articles and documents

A method for synthesizing graciousness mixed lu an

The invention discloses a novel method for compounding enzalutamide, belongs to the technical field of pharmacy synthetic technology, and particularly relates to novel technology for compounding enzalutamide. Most known methods for compounding enzalutamide relate to use of highly toxic and mephitical thiophosgene and highly toxic oxobutyronitrile, and have relatively great difficulty for industrialization. According to the invention, non-toxic and harmless thiourea and an isobutyric acid derivative are used for a reaction to obtain a key parent nucleus of 5,5-dimethyl-2-thioketone imidazole-4-ketone, and therefore, thiophosgene and oxobutyronitrile are effectively avoided. The method has a mild reaction condition, is relatively high in yield, and therefore has a great industrial prospect.

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