(Z)-dodec-9-enyl acetate, with the CAS number 16974-11-1, is an organic compound characterized by its structure as an ester derived from dodec-9-enoic acid and ethanol. This compound features a long carbon chain, which contributes to its hydrophobic nature, making it less soluble in water but more soluble in organic solvents. The presence of a double bond in the carbon chain indicates that it exhibits geometric isomerism, with the (Z) configuration denoting that the substituents on the double bond are on the same side, influencing its physical and chemical properties. Typically, (Z)-dodec-9-enyl acetate has a pleasant, fruity aroma, making it of interest in the fragrance and flavor industries. Its boiling point and melting point are influenced by the length of the carbon chain and the presence of functional groups. Additionally, it may undergo reactions typical of esters, such as hydrolysis and transesterification, under appropriate conditions. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance.

(Z)-dodec-9-enyl acetate

16974-11-1: (9Z)-Dodec-9-en-1-ol acetate, (9Z)-Dodecen-1-ol acetate, (9Z)-dodec-9-en-1-yl acetate, (Z)-1-Acetoxy-9-dodecene, (Z)-9-Dodecen-1-ol acetate, (Z)-9-Dodecen-1-yl acetate, (Z)-9-Dodecenyl acetate, (Z)-Dodec-9-en-1-yl acetate, 9-(Z)-Dodecen-1-ol acetate, 9-Dodecen-1-ol, 1-acetate, (9Z)-, 9-Dodecen-1-ol, acetate, (9Z)-, 9-Dodecen-1-ol, acetate, (Z)-, Ai3-33971, Bocep VITI, Brn 2249022, Caswell No. 411B, EPA Pesticide Chemical Code 117701, EPA Pesticide Chemical Code 129004, Eupoewit, Grapemone, Nomate Shootgard, Sonolure, WPSB Pheromone, cis-9-Dodecen-1-ol acetate, cis-9-Dodecen-1-yl acetate, cis-9-Dodecenyl acetate

Z-9-DODECEN-1-YL ACETATE

(9Z)-9-Dodecen-1-ol acetate is a synthetic compound that has been used in biological studies. It can be prepared by the reaction of hexane with 9-dodecenoic acid and is an analog of dodecanol. This compound has shown potential as a chemical pesticide, but its use is limited by the fact that it is easily degraded by light and oxygen. (9Z)-9-Dodecen-1-ol acetate has been found to have an inhibitory effect on lepidoptera, which may be due to its ability to inhibit the synthesis of proteins in these insects. The chemical analysis of this compound has been carried out using GC/MS. The geometric isomers are determined through HPLC and IR spectroscopy.

CAS 16974-11-1: (Z)-dodec-9-enyl acetate

Z-9-DODECEN-1-YL ACETATE

Ref: IN-DA00APAI

(9Z)-9-Dodecen-1-ol acetate

Ref: 3D-FD167855

(Z)-9-Dodecenyl acetate

Ref: 7W-GX8429

(Z)-9-Dodecenyl acetate

Ref: 10-F621481