869789-69-5

Basic information

• Product Name: (E)-3-(4-chlorophenyl)-1-(1-methyl-1H-imidazol-2-yl)prop-2-en-1-one
• Synonyms: (E)-3-(4-chlorophenyl)-1-(1-methyl-1H-imidazol-2-yl)prop-2-en-1-one
• CAS NO: 869789-69-5
• Molecular Weight: 246.696
• Mol File: 869789-69-5.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: (E)-3-(4-chlorophenyl)-1-(1-methyl-1H-imidazol-2-yl)prop-2-en-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3-(4-chlorophenyl)-1-(1-methyl-1H-imidazol-2-yl)prop-2-en-1-one(869789-69-5)
• EPA Substance Registry System: (E)-3-(4-chlorophenyl)-1-(1-methyl-1H-imidazol-2-yl)prop-2-en-1-one(869789-69-5)

Safety Data

• Hazardous Substances Data: 869789-69-5(Hazardous Substances Data)

Upstream product

• 85692-37-1 1-(1-methyl-1H-imidazol-2-yl)ethan-1-one 
• 104-88-1 4-chlorobenzaldehyde 

Downstream Products

• 1242049-82-6 3-(4-chlorophenyl)-3-(5-methoxy-1H-indol-3-yl)-1-(1-methyl-1H-imidazol-2-yl)propan-1-one 
• 1163795-79-6 (S)-3-(4-chlorophenyl)-3-(5-methoxy-1H-indol-3-yl)-1-(1-methyl-1H-imidazol-2-yl)propan-1-one 

Relevant articles and documents

Direct Access to Highly Enantioenriched α-Branched Acrylonitriles through a One-Pot Sequential Asymmetric Michael Addition/Retro-Dieckmann/Retro-Michael Fragmentation Cascade

A highly enantioselective synthesis of α-branched acrylonitriles is reported featuring a one-pot sequential asymmetric Michael addition/retro-Dieckmann/retro-Michael fragmentation cascade. The method, which relies on a solid, bench-stable, and commercially available acrylonitrile surrogate, is practical, scalable, and highly versatile and provides a direct access to a wide range of enantioenriched nitrile-containing building blocks. Most importantly, the method offers a new tool to incorporate an acrylonitrile moiety in an asymmetric fashion.

Expanding biohybrid-mediated asymmetric catalysis into the realm of RNA

The recent development of biohybrid catalytic systems has allowed synthetic chemists to reach high levels of selectivity on a wide variety of valuable synthetic transformations. In this context, DNA-based catalysts have emerged as particularly appealing t

DNA vs. mirror-image DNA: A universal approach to tune the absolute configuration in DNA-based asymmetric catalysis

Mirror mirror on the wall: By taking advantage of the unique structural features of L-DNA, the first examples of left-helical enantioselective induction in the field of DNA-based asymmetric catalysis were realized. Most importantly, this approach is the o