155912-06-4

Basic information

• Product Name: 1H-Indole-2-carboxaldehyde, 1-[(2-iodophenyl)methyl]-
• CAS NO: 155912-06-4
• Molecular Formula: C16H12INO
• Molecular Weight: 361.182
• Mol File: 155912-06-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1H-Indole-2-carboxaldehyde, 1-[(2-iodophenyl)methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole-2-carboxaldehyde, 1-[(2-iodophenyl)methyl]-(155912-06-4)
• EPA Substance Registry System: 1H-Indole-2-carboxaldehyde, 1-[(2-iodophenyl)methyl]-(155912-06-4)

Safety Data

• Hazardous Substances Data: 155912-06-4(Hazardous Substances Data)

Upstream product

• 19005-93-7 1H-indol-2-ylcarboxaldehyde 
• 59473-45-9 2-(chloromethyl)iodobenzene 

Downstream Products

• 1246088-87-8 methyl 2-{hydroxy[1-(2-iodobenzyl)-1H-indol-2-yl]methyl}acrylate 
• 1246088-88-9 ethyl 2-{hydroxy[1-(2-iodobenzyl)-1H-indol-2-yl]methyl}acrylate 
• 155912-07-5 ethyl 1-(2-iodobenzyl)indole-2-propenoate 

Relevant articles and documents

Morita-Baylis-Hillman reaction of indole-2-carboxaldehyde: New vistas for indole-annulated systems

DABCO-mediated Morita-Baylis-Hillman reactions of several 1-substituted-indole-2-carboxaldehydes are disclosed. It was discovered that carboethoxy or tert-butoxycarbonyl groups installed at N-1 undergo cleavage under the reaction conditions to afford 2-su

ELECTROCYCLIC RING CLOSURE OF 1-AZATRIENES AS A ROUTE TO THE INDOLONAPHTHYRIDINE RING SYSTEM

t-Methods of annelation of indole across the 1- and 2-positions have been explored using both the intramolecular Heck reaction and Dieckmann cyclisation.Two examples 5 and 7 of the title ring system have been produced by the thermal cyclisation of indole-3-carboxaldehyde oximes with an akenyl substituent at C-2.