1196876-22-8

Basic information

• Product Name: C₁₇H₁₇NO₂
• Synonyms: C₁₇H₁₇NO₂
• CAS NO: 1196876-22-8
• Molecular Weight: 267.327
• Mol File: 1196876-22-8.mol

Chemical Properties

• CAS DataBase Reference: C₁₇H₁₇NO₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₇H₁₇NO₂(1196876-22-8)
• EPA Substance Registry System: C₁₇H₁₇NO₂(1196876-22-8)

Safety Data

• Hazardous Substances Data: 1196876-22-8(Hazardous Substances Data)

Upstream product

• 98-86-2 acetophenone 
• 614-27-7 methyl 3-oxo-3-phenylpropionate 
• 100-46-9 benzylamine 

Downstream Products

• 1616563-17-7 methyl 1-benzyl-4-hydroxy-5-oxo-2-phenyl-4-(trifluoromethyl)-4,5-dihydro-1H-pyrrole-3-carboxylate 
• 150931-58-1 rac-methyl 3-(benzylamino)-3-phenylpropanoate 
• 1196876-24-0 C₂₃H₂₃NO₄ 
• 58412-48-9 diethyl 1-benzyl-2,5-dimethyl-1H-pyrrole-3,4-dicarboxylate 

Relevant articles and documents

Cross-dehydrogenative coupling between enamino esters and ketones: Synthesis of tetrasubstituted pyrroles

Tetrasubstituted pyrroles have been synthesized via the cross-dehydrogenative coupling between enamino esters and acetone. Silver carbonate proved to be an effective oxidant, and no transition metal catalyst is necessary.

Chiral lewis base catalyzed highly enantioselective reduction of N-alkyl β-enamino esters with trichlorosilane and water

First, test the water! In the presence of a chiral Lewis base catalyst 2, the supposedly moisture-unfriendly reduction system with trichlorosilane was found to be highly efficient and enantioselective when using water as an additive. For the first time, this method enables the reduction of a broad range of N-alkyl β-enamino esters 1 to give N-alkyl β-amino esters 3 in good to high yields and with excellent enantioselectivities (see scheme).