CAS Registry Number: 112501-46-9
Taxonomy: Physicochemical and Pharmacological Properties of Sesquiterpene Esters – The Bicyclic Sesquiterpene Esters – Daucanes (Carotanes) – Monoesters
C23H30O6: 402.2042
UV: 263, 292 [1]
IR: 3380, 3080, 2960, 1710, 1690, 1655, 1610, 1598, 1516, 1450, 1385, 1275, 1100, 875, 850, 780, 760, 738 [1]
MS: 402 [M]+ (0.2), 329 (0.6), 234 (10.9), 216 (2.5), 191 (32.2), 168 (201), 163 (17.9), 151 (100), 148 (45.9) [1]
1 H NMR: 0.85 (3H, d, J = 6.8, H-13), 0.97 (3H, d, J = 6.8, H-12), 1.26 (3H, s, H-14), 1.89 (3H, t, J = 1.7, H-15), 2.48 (1H, d, J = 11, H-5), 2.74 and 2.62 (2H, d, J = 15.6, H-10), 6.09 (1H, ddd, J = 2; 2.4; 11, H-6), 6.19 (1H, dd, J = 2; 2.4, H-7); OVan: 3.95 (3H, s, OCH3), 6.96 (1H, d, J = 8.4, H-5′), 7.58 (1H, d, J = 1.9, H-2′), 7.69 (1H, dd, J = 1.9; 8.4, H-6′) [1]
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
M. Miski, T.J. Mabry, J. Nat. Prod. 50, 829 (1987)
M. Miski, J. Jakupovic, Phytochemistry 29(1), 173 (1990)
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2013 Springer Science+Business Media New York
About this entry
Cite this entry
(2013). 6α-Vanilloyloxy-4β-hydroxy-5α(H)-dauc-7-en-9-one (Lancerodiol Vanillate). In: Azimova, S.S., Saidkhodzhaev, A.I. (eds) Natural Compounds. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-0539-9_931
Download citation
DOI: https://doi.org/10.1007/978-1-4614-0539-9_931
Publisher Name: Springer, New York, NY
Print ISBN: 978-1-4614-0538-2
Online ISBN: 978-1-4614-0539-9
eBook Packages: Chemistry and Materials ScienceReference Module Physical and Materials ScienceReference Module Chemistry, Materials and Physics