13857-03-9

Usage

Uses

Used in Agricultural Settings:
Z-7-Decen-1-yl Acetate is used as a pheromone for pest control purposes, specifically targeting moths and butterflies. Its ability to attract these insects helps in managing their populations and reducing the damage they cause to crops.
Used in Scientific Research:
In the field of entomology, Z-7-Decen-1-yl Acetate is used as a pheromone to study insect behavior. Researchers utilize Z-7-DECEN-1-YL ACETATE to understand the mating and communication patterns of moths and butterflies, which can provide insights into their ecology and evolution.
Used in Environmental Safety:
Despite its potent activity towards insects, Z-7-Decen-1-yl Acetate is generally considered safe for humans and the environment when used properly. This makes it a preferred choice for pest control in sensitive ecosystems where the use of harmful chemicals may have adverse effects on non-target species and the environment as a whole.

InChI:InChI=1/C12H22O2/c1-3-4-5-6-7-8-9-10-11-14-12(2)13/h4-5H,3,6-11H2,1-2H3/b5-4-

Upstream product

• 69222-08-8 7-decyn-1-ol 
• 112983-54-7 C₁₄H₃₀N₄O 
• 871-91-0 oct-7-yn-1-ol 
• 34126-19-7 4-octyne-1-ol 
• 16695-31-1 1-(2-Tetrahydropyranyloxy)-7-octyne 
• 13857-02-8 Dec-7-in-1-yl acetat 
• 112983-42-3 1-tert-Butoxy-8-hydroxydecan-7-on 
• 112983-47-8 10-tert-Butoxy-decane-3,4-dione 
• 100669-80-5 1-tert-Butoxy-dec-7-in 
• 172917-61-2 1-<(tetrahydro-2H-pyran-2-yl)oxy>-7-decyne 

Relevant academic research and scientific papers

Short and stereoselective syntheses of pheromone components of Aproaerema modicella

Efficient syntheses of pheromone components of Aproaerema modicella starting from a common intermediate 7-octyn-1-ol is described.

PRODUCTION OF FATTY OLEFIN DERIVATIVES VIA OLEFIN METATHESIS

In one aspect, the invention provides a method for synthesizing a fatty olefin derivative. The method includes: a) contacting an olefin according to Formula I with a metathesis reaction partner according to Formula IIb in the presence of a metathesis catalyst under conditions sufficient to form a metathesis product according to Formula IIIb: and b) converting the metathesis product to the fatty olefin derivative. Each R1 is independently selected from H, C1-18 alkyl, and C2-18 alkenyl; R2b is C1-8 alkyl; subscript y is an integer ranging from 0 to 17; and subscript z is an integer ranging from 0 to 17. In certain embodiments, the metathesis catalyst is a tungsten catalyst or a molybdenum catalyst. In various embodiments, the fatty olefin derivative is a pheromone. Pheromone compositions and methods of using them are also described.

Exo- and Endohormones. XI. Synthesis of Monounsaturated Sex Pheromones of Lepitoptera via α-Dicetones

α-Dicetones (5), prepared starting either with cyanohydrines (1) or with N,N-diethyl oxamate (6), were converted via the dihydrazones 11 ito acetylenes (12).Replacement of the protecting group by the acatate group and partial stereoselective reduction of the triple bond led finally to the title conpounds.