890169-52-5

Basic information

• Product Name: ethyl 2-((4-isopropylphenyl)amino)acetate
• Synonyms: ethyl 2-((4-isopropylphenyl)amino)acetate
• CAS NO: 890169-52-5
• Molecular Weight: 221.299
• Mol File: 890169-52-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: ethyl 2-((4-isopropylphenyl)amino)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-((4-isopropylphenyl)amino)acetate(890169-52-5)
• EPA Substance Registry System: ethyl 2-((4-isopropylphenyl)amino)acetate(890169-52-5)

Safety Data

• Hazardous Substances Data: 890169-52-5(Hazardous Substances Data)

Upstream product

• 623-73-4 diazoacetic acid ethyl ester 
• 99-88-7 4-Isopropylaniline 
• 109-92-2 ethyl vinyl ether 
• 105-36-2 ethyl bromoacetate 

Relevant articles and documents

Copper catalysis: One-pot simultaneous synthesis of quinolines and gem-diamine derivatives

A copper(II)-catalyzed oxidative reaction for the one-pot simultaneous synthesis of quinolines and gem-diamine derivatives from N-arylglycine ethyl esters and enamides is described. In this reaction, the two fragments in an enamide substrate react with th

MYOGLOBIN-BASED CATALYSTS FOR CARBENE TRANSFER REACTIONS

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Cytochrome P450-catalyzed insertion of carbenoids into N-H bonds

Expanding nature's catalytic repertoire to include reactions important in synthetic chemistry will open new opportunities for 'green' chemistry and biosynthesis. We demonstrate the first enzyme-catalyzed insertion of carbenoids into N-H bonds. This type of bond disconnection, which has no counterpart in nature, can be mediated by variants of the cytochrome P450 from Bacillus megaterium. The N-H insertion reaction takes place in water, provides the desired products in 26-83% yield, forms the single addition product exclusively, and does not require slow addition of the diazo component.