1361384-66-8

Basic information

• Product Name: (S)-tert-butyl α-hydroxy-α-(3-methylphenyl)acetate
• Synonyms: (S)-tert-butyl α-hydroxy-α-(3-methylphenyl)acetate
• CAS NO: 1361384-66-8
• Molecular Weight: 222.284
• Mol File: 1361384-66-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (S)-tert-butyl α-hydroxy-α-(3-methylphenyl)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-tert-butyl α-hydroxy-α-(3-methylphenyl)acetate(1361384-66-8)
• EPA Substance Registry System: (S)-tert-butyl α-hydroxy-α-(3-methylphenyl)acetate(1361384-66-8)

Safety Data

• Hazardous Substances Data: 1361384-66-8(Hazardous Substances Data)

Upstream product

• 118888-62-3 m-tolylglyoxal 
• 75-65-0 tert-butyl alcohol 
• 13994-41-7 tert-butoxycarbonylmethyl nitrate 
• 7633-32-1 tert-butyl glyoxylate 
• 17933-03-8 m-tolylboronic acid 
• 5292-43-3 bromoacetic acid tert-butyl ester 

Relevant articles and documents

Chiral N,N′-dioxide-FeCl3 complex-catalyzed asymmetric intramolecular Cannizzaro reaction

An environmentally benign catalyst, the N,N′-dioxide-FeCl3 complex, has been developed for the asymmetric intramolecular Cannizzaro reaction. Aryl and alkyl glyoxal monohydrates were applied to obtain α-hydroxy acid esters with excellent results. Deuterium-label and control experiments shed light on the reaction mechanism.