Propylure
Title: Propylure
CAS Registry Number: 10297-61-7
CAS Name: (E)-10-Propyl-5,9-tridecadien-1-ol acetate
Additional Names: trans-1-acetoxy-10-(n-propyl)trideca-5,9-diene; 10-propyl-trans-5,9-tridecadienyl acetate
Molecular Formula: C18H32O2
Molecular Weight: 280.45
Percent Composition: C 77.09%, H 11.50%, O 11.41%
Literature References: Once thought to be the sex pheromone of the pink bollworm moth, Pectinophora gossypiella (Saunders), a destructive cotton pest: H. E. Hummel et al., Science 181, 873 (1973), cf. Gossyplure. Reported as the first known natural product possessing di-n-propyl branching. Isoln, structure, and synthesis: Jones et al., Science 152, 1516 (1966). Improved total syntheses: Pattenden, J. Chem. Soc. C 1968, 2385; Meyers, Collington, Tetrahedron 27, 5979 (1971); Vig et al., J. Indian Chem. Soc. 50, 39 (1973); K. Utimoto et al., Tetrahedron Lett. 1975, 4233. Photochemical synthesis: Kossanyi et al., ibid. 1973, 3459. Stereoselective synthesis: A. Alexakis et al., ibid. 1978, 2027. trans-Propylure is rendered inactive by the presence of >15% of the cis-isomer: Jacobson, Science 163, 190 (1969).
Properties: Colorless liquid having no detectable odor. bp0.1 135°. nD25 1.4635. Strong IR band at 970 cm-1.
Boiling point: bp0.1 135°
Index of refraction: nD25 1.4635
Use: Insect attractant.

Others monographs:
n-Butyl CyanoacrylatePicoplatinsec-Butyl MercaptanAmicarbalide
PapayaBuphanamineAmmonium Tetrachloroaluminate7-Dehydrositosterol
3-Nitrosalicylic Acidα-PhellandreneCambendazoleSavin
Luteinizing HormoneMoxalactamMitotaneMetronidazole
©2016 DrugLead US FDA&EMEA