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CAS No 64726-91-6 , Japonilure

  • Name: Japonilure
  • Synonyms: Japonilure;(R,Z)-5-(1-Decenyl)dihydrofuran-2(3H)-one;
  • CAS Registry Number:
  • Density: 0.985 g/cm3
  • Refractive index: 1.512
  • EINECS: 265-035-8
  • Molecular Weight: 224.34
  • InChI: InChI=1/C14H24O2/c1-2-3-4-5-6-7-8-9-10-13-11-12-14(15)16-13/h9-10,13H,2-8,11-12H2,1H3/b10-9-/t13-/m0/s1
  • Molecular Formula: C14H24O2
  • Molecular Structure:CAS No:64726-91-6 Japonilure
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64726-91-6 2(3H)-Furanone,5-(1Z)-1-decen-1-yldihydro-, (5R)-

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64726-91-6 japonlure

  • japonlure
  • Germany CHEMOS GmbH [Manufacturer]
  • Tel: 0049 9402/9336 0
  • Fax: 0049 9402/9336 13
  • Address: CHEMOS GmbH
    Werner-von-Siemensstr. 3
    93128 Regenstauf
    Germany null,nullGermany
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64726-91-6 JAPONLURE

  • JAPONLURE
  • Hong kong Advanced Technology & Industrial Co., Ltd. [Manufacturer]
  • Tel: (852) 2390 2293/ (852) 2394 5546
  • Fax: (852) 2789 8314
  • Address: Unit B, 1/F., Cheong Shing Bldg.,
    17 Walnut St., Tai Kok Tsui, Kln,
    Hong Kong null,nullHong kong
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References of Japonilure
Title: Japonilure
CAS Registry Number: 64726-91-6
CAS Name: [R-(Z)]-5-(1-Decenyl)dihydro-2(3H)-furanone
Synonyms: [(4R,5Z)]-tetradecen-4-olide; (R,Z)-5-(dec-1-enyl)oxacyclopentan-2-one; IN-60
Molecular Formula: C14H24O2
Molecular Weight: 224.34
Percent Composition: C 74.95%, H 10.78%, O 14.26%
Literature References: Sex pheromone produced by the female Japanese beetle, Popillia japonica Newman (Coleoptera: Scarabaeidae); biological activity is inhibited by its antipode. Isoln and synthesis: J. H. Tumlinson et al., Science 197, 789 (1977). Description of attractant activity: J. H. Tumlinson in Adv. Pest. Sci., 4th Int. Congr. Pest. Chem. 2, H. Geissbühler, Ed (Pergamon Press, Oxford, England, 1979) 315-322. Use in beetle traps: T. L. Ladd, Jr., M. G. Klein, J. Econ. Entomol. 79, 84 (1986); A. Martins et al., Ecol. Bull. 39, 101 (1988). Stereospecific synthesis: S. Chattopadhyay et al., Synth. Commun. 20, 1299 (1990); T. Ebata et al., Biosci. Biotech. Biochem. 56, 818 (1992). Isolation from Anomala spp. as component of pheromone system and field evaluation: W. S. Leal et al., J. Chem. Ecol. 20, 1643 (1994); W. S. Leal et al., ibid. 1667.
Properties: bp0.1mm 130-134°. [a]D21 -69.0° (c = 1.42 in CHCl3). [a]D25 -70.2° (c = 0.5 in CHCl3).
Boiling point: bp0.1mm 130-134°
Optical Rotation: [a]D21 -69.0° (c = 1.42 in CHCl3); [a]D25 -70.2° (c = 0.5 in CHCl3)