41453-57-0

Usage

Uses

Used in the Food Industry:
(Z)-non-2-enyl acetate is used as a flavoring agent for its natural, sweet, and fruity aroma with a floral undertone. It is commonly found in fruits such as strawberries, bananas, and apples, enhancing the overall taste and scent of various food products.
Used in the Perfume Industry:
(Z)-non-2-enyl acetate is used as a key ingredient in perfumes and personal care products due to its pleasant and versatile odor. Its ability to provide a sweet and fruity fragrance makes it a valuable addition to the formulation of various scented products.
Used in the Insect World:
(Z)-non-2-enyl acetate serves as a pheromone, particularly for attracting and communicating with certain types of insects. This application takes advantage of the compound's natural occurrence in the environment and its ability to elicit specific behavioral responses from insects.

InChI:InChI=1/C11H20O2/c1-3-4-5-6-7-8-9-10-13-11(2)12/h8-9H,3-7,10H2,1-2H3/b9-8-

Upstream product

• 41453-56-9 (Z)-2-nonen-1-ol 
• 75-36-5 acetyl chloride 
• 25260-60-0 cis-1,4-bis(acetyloxy)but-2-ene 
• 111-66-0 oct-1-ene 

Downstream Products

• 7779-54-6 1-acetoxy-3-nonanone 
• 1223575-18-5 (Z)-1-chloro-4-non-2-enylsulfanyl-benzene 
• 1290670-61-9 C₁₅H₂₂Se 

Relevant academic research and scientific papers

Complete retention of Z geometry in allylic substitution catalyzed by an iridium complex

(equation presented) The Z geometry of methyl (Z)-3-monosubstituted-2-alkenyl carbonate was completely retained in iridium complex-catalyzed allylic amination. The reaction of methyl (Z)-2-nonenyl carbonate with piperidine in the presence of a catalytic amount of [Ir(COD)Cl]2 and P(OPh)3 at 50°C for 2 h gave a 98:2 mixture of (Z)-1-(2-nonenyl)piperidine and 1-(1-n-hexyl-2-propenyl)piperidine in 86percent yield. No E isomer was obtained. Various (Z)-allylic amines were obtained in 91-100percent selectivity by allylic amination of methyl (Z)-3-monosubstituted-2-alkenyl carbonate.

RUTHENIUM COMPLEXES USEFUL FOR CATALYZING METATHESIS REACTIONS

Compound of formula (4) or formula (5), wherein L is a neutral ligand, preferably a nitrogen-containing heterocyclic carbene (NHC) such as carbene containing at least two nitrogen atoms, a cyclic aminoalkyl carbene (CAAC) or a bicyclic aminoalkyl carbene (BICAAC); R1, R3, R4, R5, R6, R7, R8, R9, R10 and R11 are, independently, H, unbranched or branched C1-20 alkyl, C5-9 cycloalkyl, unbranched or branched C1-20 alkoxy, optionally bearing one or more halogen atoms, respectively; or aryl, optionally substituted with one or more of unbranched or branched C1-20 alkyl, C5-9 cycloalkyl, unbranched or branched C1-20 alkoxy, aryl, aryloxy, unbranched or branched C1-20 alkylcarbonyl, arylcarbonyl, unbranched or branched C1-20 alkoxycarbonyl, aryloxycarbonyl, heteroaryl, carboxyl, cyano, nitro, amido, aminosulfonyl, N-heteroarylsulfonyl, unbranched or branched C1-20 alkylsulfonyl, arylsulfonyl, unbranched or branched C1-20 alkylsulfinyl, arylsulfinyl, unbranched or branched C1-20 alkylthio, arylthio, sulfonamide, halogen or N(Ry)(Rz), wherein Ry and Rz are independently selected from H and C1-20 alkyl: R2 is H, unbranched or branched C1-20 alkyl.