Asarones

Title: Asarones
CAS Name: 1,2,4-Trimethoxy-5-(1-propenyl)benzene
Additional Names: 2,4,5-trimethoxy-1-propenylbenzene; asarin; asarum camphor; asarabacca camphor
Molecular Formula: C12H16O3
Molecular Weight: 208.25
Percent Composition: C 69.21%, H 7.74%, O 23.05%
Literature References: From root of Asarum europaeum L., Aristolochiaceae by distillation with water. Also found in the ethereal oils of A. europaeum and A. arifolium L., Aristolochiaceae and in Acorus calamus L., Araceae. Occurs in nature as a mixture of two isomeric forms, a-asarone being the (E)- or trans-isomer, b-asarone, the (Z)- or cis-isomer. The unqualified term asarone is often used synonymously with a-asarone. Isoln: Gattermann, Eggers, Ber. 32, 289 (1899). Early syntheses: Seshadri, Thiruvengadam, Proc. Indian Acad. Sci. 32A, 110 (1950); Sharma, Dandiya, Indian J. Appl. Chem. 32, 236 (1969). Stereochemistry of isomers: Baxter et al., Can. J. Chem. 40, 154 (1962). Insect chemosterilant activity of b-asarone: B. P. Saxena et al., Nature 270, 512 (1977); see also G. Motolesy et al., Z. Naturforsch. 35B, 1449 (1980). Stereospecific synthesis of b-asarone: M. T. S. Hsia et al., 177th Am. Chem. Soc. Meet. (Honolulu, April 1979), Abstracts of Papers, PEST 98. Synthetic and HPLC study of a- and b-asarone: L. Gracza, Arch. Pharm. 314, 972 (1981).
Derivative Type: a-Asarone
Properties: Needles from light petroleum, mp 62-63°. bp 296°. nD11 1.5719. Practically insol in water; sol in alcohol, ether, glacial acetic acid, carbon tetrachloride, chloroform, petr ether.
Melting point: mp 62-63°
Boiling point: bp 296°
Index of refraction: nD11 1.5719
Asarum Ascaridole Asclepias Ascorbic Acid Ascorbigen