57022-74-9 Usage
Description
(2E,4E)-deca-2,4-dienyl isovalerate is a colorless to pale yellow liquid chemical compound with a fruity, green, and slightly floral odor. It is commonly found in various fruits and vegetables and is used in the production of fragrances and flavors.
Uses
Used in Fragrance Industry:
(2E,4E)-deca-2,4-dienyl isovalerate is used as a fragrance ingredient for its pleasant and fruity odor. It is commonly used in perfumes, soaps, and cosmetics to add a fresh and natural scent.
Used in Food and Beverage Industry:
(2E,4E)-deca-2,4-dienyl isovalerate is used as a flavoring agent in food and beverages. It adds a sweet and fruity taste, making it a popular choice for a wide range of consumer products.
Used in Flavor and Fragrance Compounds:
(2E,4E)-deca-2,4-dienyl isovalerate is used as a key component in the creation of various flavor and fragrance compounds. Its versatility and pleasant odor make it a valuable addition to a wide range of consumer products.
Check Digit Verification of cas no
The CAS Registry Mumber 57022-74-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,0,2 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57022-74:
(7*5)+(6*7)+(5*0)+(4*2)+(3*2)+(2*7)+(1*4)=109
109 % 10 = 9
So 57022-74-9 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+
57022-74-9Relevant articles and documents
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.
