124031-17-0

Basic information

• Product Name: ETHYL 2-AMINO-2-(4-CHLOROPHENYL)ACETATE
• Synonyms: ETHYL 2-AMINO-2-(4-CHLOROPHENYL)ACETATE;Amino-(4-chloro-phenyl)-acetic acid ethyl ester
• CAS NO: 124031-17-0
• Molecular Formula: C₁₀H₁₂ClNO₂
• Molecular Weight: 213.66078
• Mol File: 124031-17-0.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: ETHYL 2-AMINO-2-(4-CHLOROPHENYL)ACETATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 2-AMINO-2-(4-CHLOROPHENYL)ACETATE(124031-17-0)
• EPA Substance Registry System: ETHYL 2-AMINO-2-(4-CHLOROPHENYL)ACETATE(124031-17-0)

Safety Data

• Hazardous Substances Data: 124031-17-0(Hazardous Substances Data)

Upstream product

• 6212-33-5 2-(4-Chlorophenyl)glycine 
• 1355333-11-7 ethyl 2-(4-chlorophenyl)-2-nitroacetate 

Downstream Products

• 1423136-88-2 ethyl 4-benzoyl-2-(4-chlorophenyl)-5-(4-nitrophenyl)-2,5-dihydro-1H-pyrrole-2-carboxylate 
• 1423136-89-3 ethyl 4-benzoyl-2-(4-chlorophenyl)-5-(4-nitrophenyl)-2,5-dihydro-1H-pyrrole-2-carboxylate 

Relevant articles and documents

Site-Selective γ-C(sp3)?H and γ-C(sp2)?H Arylation of Free Amino Esters Promoted by a Catalytic Transient Directing Group

The first selective PdII-catalysed γ-C(sp3)?H and γ-C(sp2)?H arylation of free amino esters using a commercially available catalytic transient directing group. A variety of free amino esters, including α-amino esters and β-amino esters, amino monoesters and amino bis-esters, are shown to react with a diverse range of simple aryl and heteroaryl iodide reagents.