693794-65-9

Basic information

• Product Name: 1-[2-(4-methoxyphenyl)-1H-indol-1-yl]ethanone
• Synonyms: 1-[2-(4-methoxyphenyl)-1H-indol-1-yl]ethanone
• CAS NO: 693794-65-9
• Molecular Weight: 265.312
• Mol File: 693794-65-9.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-[2-(4-methoxyphenyl)-1H-indol-1-yl]ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[2-(4-methoxyphenyl)-1H-indol-1-yl]ethanone(693794-65-9)
• EPA Substance Registry System: 1-[2-(4-methoxyphenyl)-1H-indol-1-yl]ethanone(693794-65-9)

Safety Data

• Hazardous Substances Data: 693794-65-9(Hazardous Substances Data)

Upstream product

• 768-60-5 4-methoxyphenylacetylen 
• 157869-15-3 2-((4-methoxyphenyl)ethynyl)aniline 
• 615-43-0 2-iodophenylamine 
• 1267460-48-9 N-(2-((4-methoxyphenyl)ethynyl)phenyl)acetamide 
• 20939-77-9 2-acetamidobenzyl alcohol 
• 5344-90-1 2-Aminobenzyl alcohol 
• 696-62-8 para-iodoanisole 
• 61403-29-0 N-(2-ethynylphenyl)acetamide 
• 5720-07-0 4-methoxyphenylboronic acid 
• 693794-61-5 N-[2-(2,2-dibromovinyl)-phenyl]-acetamide 

Downstream Products

• 5784-95-2 2-(4-methoxyphenyl)-1H-indole 

Relevant articles and documents

Monohydride-Dichloro Rhodium(III) Complexes with Chiral Diphosphine Ligands as Catalysts for Asymmetric Hydrogenation of Olefinic Substrates

We report full details of the synthesis and characterization of monohydride-dichloro rhodium(III) complexes bearing chiral diphosphine ligands, such as (S)-BINAP, (S)-DM-SEGPHOS, and (S)-DTBM-SEGPHOS, producing cationic triply chloride bridged dinuclear rhodium(III) complexes (1 a: (S)-BINAP; 1 b: (S)-DM-SEGPHOS) and a neutral mononuclear monohydride-dichloro rhodium(III) complex (1 c: (S)-DTBM-SEGPHOS) in high yield and high purity. Their solid state structure and solution behavior were determined by crystallographic studies as well as full spectral data, including DOSY NMR spectroscopy. Among these three complexes, 1 c has a rigid pocket surrounded by two chloride atoms bound to the rhodium atom together with one tBu group of (S)-DTBM-SEGPHOS for fitting to simple olefins without any coordinating functional groups. Complex 1 c exhibited superior catalytic activity and enantioselectivity for asymmetric hydrogenation of exo-olefins and olefinic substrates. The catalytic activity of 1 c was compared with that of well-demonstrated dihydride species derived in situ from rhodium(I) precursors such as [Rh(cod)Cl]2 and [Rh(cod)2]+[BF4]? upon mixing with (S)-DTBM-SEGPHOS under dihydrogen.

Multicatalytic one-pot reaction of 1-(2-alkynylphenyl)ketoximes for generation of indole derivatives

Multicatalytic one-pot Beckmann rearrangement/intramolecular cyclization/halogenation reaction of 1-(2-alkynylphenyl)ketoxime is reported, leading to the expected indole derivatives in good yield.

Copper(I)-catalyzed coupling of terminal acetylenes with aryl or vinyl halides

Synthetic protocols using copper(I) catalysts for the formation of diaryl acetylenes, 1,3-enynes, benzofurans and indoles are described. Georg Thieme Verlag Stuttgart.