1242049-84-8

Basic information

• Product Name: 3-(5-methoxy-1H-indol-3-yl)-3-(4-methoxyphenyl)-1-(1-methyl-1H-imidazol-2-yl)propan-1-one
• Synonyms: 3-(5-methoxy-1H-indol-3-yl)-3-(4-methoxyphenyl)-1-(1-methyl-1H-imidazol-2-yl)propan-1-one
• CAS NO: 1242049-84-8
• Molecular Weight: 389.454
• Mol File: 1242049-84-8.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 3-(5-methoxy-1H-indol-3-yl)-3-(4-methoxyphenyl)-1-(1-methyl-1H-imidazol-2-yl)propan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(5-methoxy-1H-indol-3-yl)-3-(4-methoxyphenyl)-1-(1-methyl-1H-imidazol-2-yl)propan-1-one(1242049-84-8)
• EPA Substance Registry System: 3-(5-methoxy-1H-indol-3-yl)-3-(4-methoxyphenyl)-1-(1-methyl-1H-imidazol-2-yl)propan-1-one(1242049-84-8)

Safety Data

• Hazardous Substances Data: 1242049-84-8(Hazardous Substances Data)

Upstream product

• 869789-73-1 (E)-3-(2-bromophenyl)-1-(1-methyl-1H-imidazol-2-yl)prop-2-en-1-one 
• 1006-94-6 5-methoxylindole 
• 869789-68-4 (E)-3-(4-methoxyphenyl)-1-(1-methyl-1H-imidazol-2-yl)prop-2-en-1-one 
• 85692-37-1 1-(1-methyl-1H-imidazol-2-yl)ethan-1-one 

Relevant articles and documents

Guanosine-based self-assembly as an enantioselective catalyst scaffold

A self-assembled G-quadruplex formed by guanosine and borate as the chiral scaffold was used to catalyze the asymmetric Friedel-Crafts reaction in water. Catalysis, depending on the self-assembly of guanosine and borate into a fibrillar structure in the p

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