724707-89-5

Basic information

• Product Name: 4-phenylcyclohex-3-en-1-one ethylene glycol ketal
• Synonyms: 4-phenylcyclohex-3-en-1-one ethylene glycol ketal
• CAS NO: 724707-89-5
• Molecular Weight: 216.28
• Mol File: 724707-89-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 4-phenylcyclohex-3-en-1-one ethylene glycol ketal(CAS DataBase Reference)
• NIST Chemistry Reference: 4-phenylcyclohex-3-en-1-one ethylene glycol ketal(724707-89-5)
• EPA Substance Registry System: 4-phenylcyclohex-3-en-1-one ethylene glycol ketal(724707-89-5)

Safety Data

• Hazardous Substances Data: 724707-89-5(Hazardous Substances Data)

Upstream product

• 124941-13-5 8-phenylthio-1,4-dioxaspiro[4,5]decane 
• 100-58-3 phenylmagnesium bromide 
• 3262-89-3 triphenylboroxine 
• 4746-97-8 cyclohexanedione monoethylene ketal 
• 170011-47-9 1,4-dioxaspiro[4.5]dec-7-en-8-yl trifluoromethanesulfonate 
• 98-80-6 phenylboronic acid 
• 108-86-1 bromobenzene 
• 680596-79-6 4,4,5,5-tetramethyl-2-(1,4-dioxaspiro[4.5]dec-7-en-8-yl)-1,3,2-dioxaborolane 
• 94112-58-0 4-hydroxy-4-phenyl-cyclohexanone ethylene ketal 

Downstream Products

• 25163-93-3 8-phenyl-1,4-dioxaspiro[4,5]decane 
• 4894-75-1 1-phenyl-4-cyclohexanone 

Relevant articles and documents

INHIBITORS OF INDOLEAMINE 2,3-DIOXYGENASE AND METHODS OF THEIR USE

There are disclosed compounds that modulate or inhibit the enzymatic activity of indoleamine 2,3-dioxygenase (IDO), pharmaceutical compositions containing said compounds and methods of treating proliferative disorders, such as cancer, viral infections and/or inflammatory disorders utilizing the compounds of the disclosure.

Catalytic asymmetric hydrogenation of α-arylcyclohexanones and total synthesis of (-)-α-lycorane

An efficient catalytic asymmetric hydrogenation of racemic α-arylcyclohexanones with an ethylene ketal group at the 5-position of the cyclohexane ring via dynamic kinetic resolution has been developed, giving chiral α-arylcyclohexanols with two contiguous

Nickel-catalyzed alkenylative cross-coupling reaction of alkyl sulfides

A novel cross-coupling reaction of alkyl aryl sulfides with aryl Grignard reagents has been achieved to produce the alkenyl-aryl coupling products in high yields by using catalytic Ni(cod)2 and a bulky N-heterocyclic carbene ligand, SIPr.