874945-80-9

Usage

General Description

2-amino-2-(anthracen-9-yl)ethanol is a chemical compound with a molecular formula C17H15NO. It is a derivative of anthracene, containing a hydroxyl group and an amino group. 2-amino-2-(anthracen-9-yl)ethanol is used in various chemical and pharmaceutical applications, such as a building block for the synthesis of organic compounds and as a fluorescent probe in biological and chemical research. It is also used in the production of dyes, plastics, and as a reagent in chemical reactions. 2-amino-2-(anthracen-9-yl)ethanol is known for its high stability and low toxicity, making it a versatile and valuable compound in the chemical industry.

Upstream product

• 120-12-7 anthracene 
• 61695-73-6 1-(9-anthryl)-ethylene oxide 
• 1284239-97-9 2-azido-2-(anthracen-9-yl)ethanol 
• 60242-00-4 methyl 2-(9-anthryl)-2-(benzyloxycarbonylamino)acetate 
• 874912-74-0 2-(9-anthryl)-2-[(benzyloxycarbonyl)amino]ethanol 

Relevant academic research and scientific papers

Determining the enantioselectivity of chiral catalysts by mass spectrometric screening of their racemic forms

The enantioselectivity of a chiral catalyst can be determined from its racemic form by mass spectrometric screening of a nonequal mixture of two mass-labeled quasienantiomeric substrates. The presented method opens up new possibilities for evaluating catalyst structures that are not readily available in enantiomerically pure form.

Effects of extended aryl-substituted bisoxazoline ligands in asymmetric synthesis - Efficient synthesis and application of 4,4′-bis(1-naphthyl)-, 4,4′-bis(2-naphthyl)- and 4,4′-bis(9-anthryl)-2,2′- isopropylidenebis(1,3-oxazolines)

The steric influence of extended aryl substituents on 2,2′-bis(1,3- oxazollne) ligands was investigated in a series of asymmetric catalytic reactions such as Mukaiyama aldol and Michael reactions, hetero-Diels-Alder processes, and allylic alkylation react