778625-56-2

Basic information

• Product Name: Phenol, 2-[[[(1R)-1-(hydroxymethyl)-2,2-dimethylpropyl]imino]methyl]-4,6-diiodo-
• CAS NO: 778625-56-2
• Molecular Formula: C13H17I2NO2
• Molecular Weight: 473.092
• Mol File: 778625-56-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Phenol, 2-[[[(1R)-1-(hydroxymethyl)-2,2-dimethylpropyl]imino]methyl]-4,6-diiodo-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 2-[[[(1R)-1-(hydroxymethyl)-2,2-dimethylpropyl]imino]methyl]-4,6-diiodo-(778625-56-2)
• EPA Substance Registry System: Phenol, 2-[[[(1R)-1-(hydroxymethyl)-2,2-dimethylpropyl]imino]methyl]-4,6-diiodo-(778625-56-2)

Safety Data

• Hazardous Substances Data: 778625-56-2(Hazardous Substances Data)

Upstream product

• 2631-77-8 3,5-diodosalicylaldehyde 
• 112245-13-3 (S)-tert-leucinol 
• 3907-02-6 (2R)-2-amino-3,3-dimethylbutan-1-ol 

Relevant articles and documents

On the Origins of Nonradiative Excited State Relaxation in Aryl Sulfoxides Relevant to Fluorescent Chemosensing

We provide herein a mechanistic analysis of aryl sulfoxide excited state processes, inspired by our recent report of aryl sulfoxide based fluorescent chemosensors. The use of aryl sulfoxides as reporting elements in chemosensor development is a significan

Copper-catalyzed asymmetric oxidation of sulfides

Copper-catalyzed asymmetric sulfoxidation of aryl benzyl and aryl alkyl sulfides, using aqueous hydrogen peroxide as the oxidant, has been investigated. A relationship between the steric effects of the sulfide substituents and the enantioselectivity of th

Enantioselective vanadium-catalyzed oxidation of 1,3-dithianes from aldehydes and ketones using β-amino alcohol derived schiff base ligands

The asymmetric vanadium-catalyzed oxidation of 1,3-dithianes from aldehydes and ketones by β-amino alcohol-derived Schiff base ligands with two stereogenic centers was investigated. Using aqueous hydrogen peroxide as the oxidant and the Schiff base 3b as