15960-82-4

Basic information

• Product Name: ethyl 3-((2,6-dimethylphenyl)amino)-3-oxopropanoate
• Synonyms: ethyl 3-((2,6-dimethylphenyl)amino)-3-oxopropanoate
• CAS NO: 15960-82-4
• Molecular Weight: 235.283
• Mol File: 15960-82-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: ethyl 3-((2,6-dimethylphenyl)amino)-3-oxopropanoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 3-((2,6-dimethylphenyl)amino)-3-oxopropanoate(15960-82-4)
• EPA Substance Registry System: ethyl 3-((2,6-dimethylphenyl)amino)-3-oxopropanoate(15960-82-4)

Safety Data

• Hazardous Substances Data: 15960-82-4(Hazardous Substances Data)

Upstream product

• 87-62-7 2,6-dimethylaniline 
• 105-53-3 diethyl malonate 
• 119072-54-7 2,6-dimethylphenyl isonitrile 
• 105-36-2 ethyl bromoacetate 
• 201230-82-2 carbon monoxide 
• 623-48-3 ethyl iodoacetae 
• 1071-46-1 hydrogen ethyl malonate 

Downstream Products

• 100616-40-8 N-(2,6-dimethyl-phenyl)-2-hydroxyimino-malonamic acid ethyl ester 
• 102881-97-0 2-amino-N-(2,6-dimethyl-phenyl)-malonamic acid ethyl ester 
• 15883-20-2 2',6'-pipecoloxylidide 
• 15960-97-1 2-Bromo-2-ethoxycarbonylaceto-2',6'-xylidid 
• 15961-01-0 2-Carbamoylaceto-2',6'-xylidid 
• 15961-02-1 2-Bromo-2-carbamoylaceto-2',6'-xylidid 

Relevant articles and documents

Novel method for preparing pilsicainide hydrochloride

The invention discloses a preparation method of pilsicainide hydrochloride. The preparation method comprises the following steps of: by taking 2, 6-dimethylaniline as a raw material, carrying out amidation reaction on the 2, 6-dimethylaniline and a compou

Transformations of Isonitriles with Bromoalkanes Using Photoredox Gold Catalysis

Isonitriles have excellent electronic compatibility to react with free radicals. Recently, photoredox catalysis has emerged as a powerful tool for the construction of C-C bonds with few protocols for alkylative heterocycle synthesis through isonitrile addition. Herein, we describe the photocatalytic generation of alkyl radicals from unactivated bromoalkanes as part of an efficient cross-coupling strategy for the diversification of isonitriles using a dimeric gold(I) photoredox catalyst, [Au2(dppm)2]Cl2.

Local anesthetics with enhanced affinity for proteins.

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