Chirality & Odour Perception
John C. Leffingwell, Ph.D.

The Ethyl (5,5-dimethylcyclohex-2-en-1-yl)acetates

You must have Java installed to view the molecular visualization on this page

Photo by permission of M. Roudintska - Art & Parfum

c

(+)-Ethyl [(1S)-5,5-dimethylcyclohex-2-en-1-yl]acetate - Odor description: Medium–intensive, pleasant, clear, sweet, ripe pear

Ref: Win'ska, K., Kula, J. and Wawrzen'czyk, C. (2011), Synthesis and odour characteristics of racemic and optically active oxy-derivatives of gem-dimethylcyclohexene. Flavour and Fragrance Journal, 26: n/a. doi: 10.1002/ffj.2049, published online: 18 March 2011

c

 

(-)-Ethyl [(1R)-5,5-dimethylcyclohex-2-en-1-yl]acetate - Odor description: Weaker than the racemate and the (S)-enantiomer, fruity, less sweet

Ref: Win'ska, K., Kula, J. and Wawrzen'czyk, C. (2011), Synthesis and odour characteristics of racemic and optically active oxy-derivatives of gem-dimethylcyclohexene. Flavour and Fragrance Journal, 26: n/a. doi: 10.1002/ffj.2049, published online: 18 March 2011

Cyclic Terpenoid Odorants

Bicyclic Terpenoid Odorants

Acyclic Terpenoid Odorants

Ionones, Irones, Damascones & Structurally Related Odorants

Acyclics (Alcohols, Esters, Acids, Aldehydes)

Lactones

Sesquiterpenoid Related Odorants

Steroid Urine Type Odorants

Sandalwood Type Odorants

Musk Odorants

Miscellaneous

HOME

Copyright 2001-2002 - Leffingwell & Associates