97567-79-8

Basic information

• Product Name: 2-OxazolaMine, 4-(1,1-diMethylethyl)-
• Synonyms: 2-OxazolaMine, 4-(1,1-diMethylethyl)-;2-aMino-4-t-butyloxazole;4-(tert-Butyl)oxazol-2-aMine
• CAS NO: 97567-79-8
• Molecular Formula: C₇H₁₂N₂O
• Molecular Weight: 140.18298
• Mol File: 97567-79-8.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-OxazolaMine, 4-(1,1-diMethylethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-OxazolaMine, 4-(1,1-diMethylethyl)-(97567-79-8)
• EPA Substance Registry System: 2-OxazolaMine, 4-(1,1-diMethylethyl)-(97567-79-8)

Safety Data

• Hazardous Substances Data: 97567-79-8(Hazardous Substances Data)

Usage

General Description

2-Oxazolamine, 4-(1,1-dimethylethyl)- is a chemical compound with the molecular formula C8H14N2O. It is a derivative of oxazolamine and is also known by its alternate name tert-butyl 4-oxazolidinecarboxylate. 2-OxazolaMine, 4-(1,1-diMethylethyl)- is commonly used as a building block in organic synthesis and pharmaceutical research due to its versatile reactivity and potential for biological activity. It can also be used in the production of various pharmaceuticals and agrochemicals. Additionally, it has been studied for its potential antimicrobial and anticancer properties, making it a focus of research in medicinal chemistry.

Upstream product

• 38895-88-4 1-hydroxy-3,3-dimethylbutan-2-one 
• 420-04-2 CYANAMID 

Downstream Products

• 97600-12-9 2-amino-4-t-butyl-N-methyloxazole-5-carbothioamide 
• 97600-11-8 N-(4-t-butyloxazol-2-yl)-N'-methylthiourea 
• 97625-92-8 N-<4-t-butyl-5-(methylthiocarbamoyl)oxazol-2-yl>-N'-methylthiourea 
• 6794-69-0 4-phenyl-1,3-dihydro-imidazol-2-one 

Relevant articles and documents

INHIBITION OF P38 KINASE ACTIVITY USING SUBSTITUTED HETEROCYCLIC UREAS

This invention relates to the use of a group of aryl ureas in treating cytokine mediated diseases, other than cancer and proteolytic enzyme mediated diseases, other than cancer, and pharmaceutical compositions for use in such therapy.

Formation of Thioamide Derivatives from Reactions of Isothiocyanates with Oxazol-2-amines

4-Substituted oxazol-2-amines react with isothiocyanates to give products having a thioamide function at C5.The reaction is considered to be an electrophilic process in competition with the usual reaction of the amino group with the isothiocyanate.The nature of the isothiocyanate and the type of substituent at C4 affect the amount of the thioamide product formed.Some chemical properties of the thioamides are also investigated.