56699-32-2 Usage
Uses
Used in Flavor and Fragrance Industry:
(2E,4Z)-Deca-2,4-dienyl isovalerate is used as a flavoring agent in the production of various food and beverage products. Its strong, unpleasant odor adds a unique taste and aroma to these products, enhancing their overall sensory experience.
Used in Perfume and Scented Product Manufacturing:
(2E,4Z)-Deca-2,4-dienyl isovalerate is used as a component in the manufacturing of perfumes and scented products. Its distinct odor contributes to the creation of various fragrances, providing a wide range of scent profiles for different applications.
Used in Food and Beverage Production:
(2E,4Z)-Deca-2,4-dienyl isovalerate is used as a flavoring agent in the production of various food and beverage products. Its unique taste and aroma enhance the sensory experience of these products, making them more appealing to consumers.
Used in Natural Food Sources:
(2E,4Z)-Deca-2,4-dienyl isovalerate is found naturally in some foods, contributing to their distinct taste and aroma. Its presence in these natural sources highlights its role in enhancing the sensory experience of food consumption.
Check Digit Verification of cas no
The CAS Registry Mumber 56699-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,9 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 56699-32:
(7*5)+(6*6)+(5*6)+(4*9)+(3*9)+(2*3)+(1*2)=172
172 % 10 = 2
So 56699-32-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H26O2/c1-4-5-6-7-8-9-10-11-12-17-15(16)13-14(2)3/h8-11,14H,4-7,12-13H2,1-3H3/b9-8-,11-10+
56699-32-2Relevant academic research and scientific papers
Structural Dynamics of Pentadienyl Metal-Compounds Bearing a Terminal Alkyl Substituent: Both 'Stereoselective' and 'Stereodefensive' Synthesis of a Natural Perfume
Bosshardt, Herbert,Schlosser, Manfred
, p. 2393 - 2403 (2007/10/02)
The (2Z,4E)-, (2E,4Z)- and (2E,4E)-isomers of 2,4-decandien-1-ol (5) have been obtained with high and predictable stereochemical homogeneity starting from both (Z)- and (E)-1,4-decadiene.These hydrocarbons were hydroxylated in a reaction sequence consisting of metallation (by means of s-butyllithium or butyllithium/potassium-t-butoxide, giving rise to organometallic intermediates of specific conformations), dimethoxyborylation and oxidation.The different decadienols as well as (2E,4Z)-2,4-undecadien-1-ol were converted into the isovalerates, the ester derived from (2E,4Z)-2,4-decadien-1-ol being a natural flavor component.
