1042737-42-7

Basic information

• Product Name: 3-(1-methyl-1H-indol-3-yl)-1-phenylpropan-1-one
• Synonyms: 3-(1-methyl-1H-indol-3-yl)-1-phenylpropan-1-one
• CAS NO: 1042737-42-7
• Molecular Weight: 263.339
• Mol File: 1042737-42-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-(1-methyl-1H-indol-3-yl)-1-phenylpropan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(1-methyl-1H-indol-3-yl)-1-phenylpropan-1-one(1042737-42-7)
• EPA Substance Registry System: 3-(1-methyl-1H-indol-3-yl)-1-phenylpropan-1-one(1042737-42-7)

Safety Data

• Hazardous Substances Data: 1042737-42-7(Hazardous Substances Data)

Upstream product

• 603-76-9 1-methylindole 
• 1504-58-1 3-Phenyl-2-propyn-1-ol 
• 55563-72-9 3-methoxy-1-phenylpropan-1-one 
• 34008-71-4 3-ethoxy-1-phenyl-1-propanone 
• 93-55-0 1-phenyl-propan-1-one 

Relevant articles and documents

Pd-Catalyzed Intramolecular Cyclization via Direct C-H Addition to Nitriles: Skeletal Diverse Synthesis of Fused Polycyclic Indoles

The first example of Pd-catalyzed intramolecular C-H addition of indoles bearing cyanohydrin components at the C(3), C(2), and N(1) positions to nitriles is described. A wide range of functionalized partially saturated carbazoles, tetrahydropyrido[1,2-a]indole, and carbazoles can be prepared in good to excellent yields under the optimal conditions. In addition, fused polycyclic indoles with seven- or eight-membered rings can also be formed smoothly.

Cu-catalyzed β-functionalization of saturated ketones with indoles: A one-step synthesis of C3-substituted indoles

An effective one-pot synthesis of β-indolylketones from saturated ketones and indoles was developed. It is noteworthy that this methodology has a good functional group tolerance (alkyl, nitro, halogen, hydroxyl, methoxyl, carboxyl and ester) and is of great significance to the preparation of many indole heterocycles.