38713-13-2

Usage

InChI:InChI=1/C13H28O/c1-11(2)7-5-8-12(3)9-6-10-13(4)14/h11-14H,5-10H2,1-4H3

Upstream product

• 141-10-6 pseudoionone 
• 1604-34-8 6,10-dimethyl-undecan-2-one 
• 689-67-8 pseudo-ionone 
• 141-10-6 pseudoionone 
• 76-05-1 trifluoroacetic acid 

Downstream Products

• 1115-94-2 2,6,10-Trimethyl-undecansaeure 

Relevant academic research and scientific papers

METHOD FOR THE PRODUCTION OF TETRAHYDROGERANYLACETONE

A method for the production of tetrahydrogeranylacetone is disclosed, whereby pseudoionone, geranylacetone and/or dihydrogeranylacetone in the liquid phase, in which particles of a catalyst, for the preferential hydrogenation of carbon-carbon double bonds before carbon-oxygen double bonds, are suspended, is fed through a device along in the presence of a gas comprising hydrogen, said device preventing the transport of the catalyst particles.

Synthesis and some reactions of isopropyl (4E,6E)-3,7,11-trimethyl-2,4,6,10-dodecatetraenoate

Starting from the condensation product of citral with acetone, isopropyl (4E,6E)-3,7,11-trimethyl-2,4,6,10-dodecatetraenoate was synthesized and some its reactions were studied.

catalysed Transfer Hydrogenation of Ketones and Aldehydes by Propan-2-ol

In the presence of the cocatalyst NaOH, catalyses efficiently the transfer hydrogenation of aliphatic and aromatic ketones and aldehydes in high yields.