16623-22-6

Basic information

• Product Name: Benzeneacetic acid, a-oxo-, 3,3,5-trimethylcyclohexyl ester
• Synonyms: 3,3,5-Trimethylcyclohexylphenylglyoxylat;Oxo-phenyl-acetic acid 3,3,5-trimethyl-cyclohexyl ester;Phenyl-glyoxylsaeure-(3,3,5-trimethyl-cyclohexylester)
• CAS NO: 16623-22-6
• Molecular Formula: C17H22O3
• Molecular Weight: 274.36
• Mol File: 16623-22-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 145 °C (0.05 mmHg)
• CAS DataBase Reference: Benzeneacetic acid, a-oxo-, 3,3,5-trimethylcyclohexyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneacetic acid, a-oxo-, 3,3,5-trimethylcyclohexyl ester(16623-22-6)
• EPA Substance Registry System: Benzeneacetic acid, a-oxo-, 3,3,5-trimethylcyclohexyl ester(16623-22-6)

Safety Data

• Hazardous Substances Data: 16623-22-6(Hazardous Substances Data)

Upstream product

• 116-02-9 3,3,5-trimethylcyclohexanol 
• 611-73-4 Benzoylformic acid 

Downstream Products

• 456-59-7 cyclandelate 

Relevant articles and documents

Cobalt-Catalyzed Transfer Hydrogenation of α-Ketoesters and N-Cyclicsulfonylimides Using H2O as Hydrogen Source

A Co-catalyzed effective transfer hydrogenation of various α-ketoesters and N-cyclicsulfonylimides by safe and environmentally benign H2O as hydrogen source is described. The reaction used easily available and easy to handle zinc metal as a reductant. Interestingly, the catalytic system does not require ligand for reduction of N-cyclicsulfonylimides. (Figure presented.).