183059-24-7

Basic information

• Product Name: Carbamic acid, (2-hydroxy-2-methylpropyl)-, 1,1-dimethylethyl ester (9CI)
• Synonyms: Carbamic acid, (2-hydroxy-2-methylpropyl)-, 1,1-dimethylethyl ester (9CI);tert-butyl 2-hydroxy-2-MethylpropylcarbaMate;(2-Hydroxy-2-methylpropyl)carbamic acid tert-butyl ester;N-Boc-(2-hydroxy-2-methyl)propylamine;Carbamic acid, N-(2-hydroxy-2-methylpropyl)-, 1,1-dimethylethyl ester
• CAS NO: 183059-24-7
• Molecular Formula: C₉H₁₉NO₃
• Molecular Weight: 189.25206
• Product Categories: N-BOC
• Mol File: 183059-24-7.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: Carbamic acid, (2-hydroxy-2-methylpropyl)-, 1,1-dimethylethyl ester (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, (2-hydroxy-2-methylpropyl)-, 1,1-dimethylethyl ester (9CI)(183059-24-7)
• EPA Substance Registry System: Carbamic acid, (2-hydroxy-2-methylpropyl)-, 1,1-dimethylethyl ester (9CI)(183059-24-7)

Safety Data

• Hazardous Substances Data: 183059-24-7(Hazardous Substances Data)

Usage

General Description

Carbamic acid, (2-hydroxy-2-methylpropyl)-, 1,1-dimethylethyl ester (9CI) is a chemical compound that falls under the category of esters, which are organic compounds made by replacing the hydrogen of an acid by an alkyl or other organic group. This specific compound is derived from the reaction between carbamic acid and 2-hydroxy-2-methylpropyl. Its structure includes a carbamic acid group (NH2COOH), a 2-hydroxy-2-methylpropyl group, and a 1,1-dimethylethyl ester group. Its molecular formula is C9H19NO3. Due to its chemical structure, it may have various potential applications in chemical research and industries. The details about its uses, hazards, or safety measures are not typically available and might require specific testing and investigations.

Upstream product

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• 74-88-4 methyl iodide 
• 75-16-1 methylmagnesium bromide 

Downstream Products

• 879001-62-4 tert-butyl 2-fluoro-2-methylpropylcarbamate 
• 223906-39-6 N-Benzyl-5,5-dimethyloxazolidin-2-one 
• 223906-48-7 N-Propionyl-5,5-dimethyloxazolidin-2-one 
• 250607-19-3 3-(2'-benzylpent-4'-enoyl)-5,5-dimethyloxazolidin-2-one 
• 250607-20-6 3-(1'-hydroxy-2'-benzylpropyl)-5,5-dimethyloxazolidin-2-one 
• 250607-16-0 3-(1'-hydroxy-3'-phenylpropyl)-5,5-dimethyloxazolidin-2-one 
• 250607-11-5 3-(3'-phenylpropionyl)-5,5-dimethyloxazolidin-2-one 
• 223906-54-5 N-(2-Methyl-1-oxo-3-phenylpropyl)-5,5-dimethyloxazolidin-2-one 

Relevant articles and documents

INHIBITORS OF BETA-SECRETASE

The present invention relates to spirocyclic acylguanidines and their use as inhibitors of the β-secretase enzyme (BACE1) activity, pharmaceutical compositions containing the same, and methods of using the same as therapeutic agents in the treatment of neurodegenerative disorders, disorders characterized by cognitive decline, cognitive impairment, dementia and diseases characterized by production of β-amyloid aggregates.

N-Phosphoryl oxazolidinones as effective phosphorylating agents

A number of N-phosphoryl oxazolidinones have been prepared and evaluated, the best being 5,5-diphenyl oxazolidinones, the utility of which was demonstrated in the phosphorylation of a number of representative primary, secondary, tertiary, and phenolic alcohols.

Asymmetric alkylations using SuperQuat auxiliaries - An investigation into the synthesis and stability of enolates derived from 5,5-disubstituted oxazolidin-2-ones

Studies on the alkylation of enolates derived from a range of N-acyl-5,5-dimethyloxazolidin-2-ones and N-acyl-5,5-diphenyloxazolidin-2-ones reveal that high yields and high diastereoselectivities are best obtained when homochiral 4-isopropyl-5,5-dimethyloxazolidin-2-one is employed as a chiral auxiliary.