69668-85-5 Usage
Uses
Used in the Food and Beverage Industry:
(Z)-3-Octenoic acid methyl ester is used as a flavoring agent for its fruity and pleasant aroma, enhancing the taste and smell of various food and drink products.
Used in the Perfume and Fragrance Industry:
(Z)-3-Octenoic acid methyl ester is also utilized in the production of perfumes and fragrances, where its unique scent contributes to the creation of appealing and long-lasting scents.
Used in Pharmaceutical Applications:
(Z)-3-Octenoic acid methyl ester serves as an intermediate in the synthesis of various organic compounds for pharmaceutical applications, playing a crucial role in the development of new medications.
Used in Agricultural Applications:
In the agricultural sector, (Z)-3-Octenoic acid methyl ester is employed as an intermediate in the synthesis of specific organic compounds, which can be used in the development of products such as pesticides or other agrochemicals.
Safety Precautions:
It is important to handle (Z)-3-Octenoic acid methyl ester with care, as it can be irritating to the eyes, skin, and respiratory system. Proper safety measures should be taken to minimize potential health risks during its use and handling.
Check Digit Verification of cas no
The CAS Registry Mumber 69668-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,6,6 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 69668-85:
(7*6)+(6*9)+(5*6)+(4*6)+(3*8)+(2*8)+(1*5)=195
195 % 10 = 5
So 69668-85-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O2/c1-3-4-5-6-7-8-9(10)11-2/h6-7H,3-5,8H2,1-2H3/b7-6-
69668-85-5Relevant academic research and scientific papers
Formation of Unsaturated Esters in the Single Electron Transfer Reaction of Cyclopropanone Acetals with Quinones under Non-irradiated Conditions
Abe, Manabu,Oku, Akira
, p. 3551 - 3554 (2007/10/02)
Unsaturated esters were formed from cyclopropanone aceytals in the reaction with DDQ or chloranil, where ring-opened C-C and C-O bonded adducts were the intermediates formed via a SET mechanism resulting in the ester formation.
Prostaglandins and Prostaglandin Intermediates. 22 - Synthesis of a Stable Prostacyclin Analogue
Theil, F.,Costisella, B.,Hauser, A.,Schick, H.,Schwarz, S.
, p. 766 - 774 (2007/10/02)
An industrially available prostaglandin intermediate is converted into a new prostacyclin analogue with a cyclic ether instead of the unstable enol ether system.For the construction of the modified alkyl side chain two subsequent Horner olefinations are used.This reaction sequence includes a new methodology for the conversion of an aldehyde into a β,γ-unsaturated carboxylic acid by a three-carbon elongation.
