65035-34-9|Lineatin|(1R,2S,5R,7R)-1,3,3-trimethyl-4,6-dioxatricyclo[3.3.1.02,7]nonane|-范德生物科技公司

Lineatin

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names：
(1R,2S,5R,7R)-1,3,3-trimethyl-4,6-dioxatricyclo[3.3.1.02,7]nonane
CAS号：
65035-34-9
MDL Number：
MF(分子式)： C10H16O2 MW(分子量)： 168.236
EINECS: Reaxys Number:
Pubchem ID: Brand:BIOFOUNT

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中文别名	Lineatin
英文别名	Lineatin
CAS号	65035-34-9
Inchi	InChI=1S/C10H16O2/c1-9(2)8-6-4-10(8,3)5-7(11-6)12-9/h6-8H,4-5H2,1-3H3/t6-,7-,8+,10-/m1/s1
InchiKey	SHTFZHTWSLHVEB-BDNRQGISSA-N
分子式 Formula	C10H16O2
分子量 Molecular Weight	168.236
溶解度Solubility
性状	Solid powder
储藏条件 Storage conditions	Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).

产品说明	Lineatin(CAS:65035-34-9):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。
Introduction	Lineatin is a pheromone isolated from the frass of the female ambrosia beetle Trypodendron lineatum Olivier, which is a deleterious pest to coniferous forests in Europe and North America.
Application1
Application2
Application3

警示图
危险性	Warning
危险性警示
安全声明
安全防护
备注

[1]Salom SM, McLean JA. Flight and landing behavior ofTrypodendron lineatum (Coleoptera: Scolytidae) in response to different semiochemicals. J Chem Ecol. 1990 Aug;16(8):2589-604. doi: 10.1007/BF0101748[1]PubMed PMID: 24264223.

[2]Shore TL, Lindgren BS. Effect of ethanol and α-pinene on response of ambrosia beetle,Trypodendron lineatum, to lineatin-baited funnel and drainpipe traps. J Chem Ecol. 1996 Dec;22(12):2187-96. doi: 10.1007/BF02029539. PubMed PMID: 24227296.

[3] Alibés R, de March P, Figueredo M, Font J, Racamonde M, Parella T. Highly efficient and diastereoselective synthesis of (+)-lineatin. Org Lett. 2004 Apr 29;6(9):1449-52. PubMed PMID: 15101764.

[4] Pérez L, Alibés R, de March P, Busqué F, Figueredo M, Font J. Stereodivergent synthesis of (+)- and (-)-isolineatin. J Org Chem. 2013 May 3;78(9):4483-9. doi: 10.1021/jo400487y. Epub 2013 Apr 22. PubMed PMID: 23581881.

[5] Racamonde M, Alibés R, Figueredo M, Font J, de March P. Photochemical cycloaddition of mono-, 1,1-, and 1,2-disubstituted olefins to a chiral 2(5H)-furanone. Diastereoselective synthesis of (+)-lineatin. J Org Chem. 2008 Aug 1;73(15):5944-52. doi: 10.1021/jo800970u. Epub 2008 Jul 8. PubMed PMID: 18605755.

6: Keeling CI, Ngo HT, Benusic KD, Slessor KN. Preparative chiral liquid chromatography for enantiomeric separation of pheromones. J Chem Ecol. 2001 Mar;27(3):487-97. PubMed PMID: 11441440.7: Mori K. [Synthesis and biological activity of optically active insect pheromones]. Yakugaku Zasshi. 1982 Oct;102(10):899-910. Review. Japanese. PubMed PMID: 6762413.

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