16824-14-9 Usage
Description
3-Methylbuta-1,3-dien-2-yl acetate, commonly known as isoprenyl acetate, is an organic compound that appears as a colorless liquid with a fruity odor. It is a derivative of isoprene and features a five-carbon backbone with an acetate group attached to the second carbon and double bonds on the first and third carbons. 3-Methylbuta-1,3-dien-2-yl acetate exhibits relative stability but can polymerize when exposed to light or heat.
Uses
Used in Flavoring Agents:
3-Methylbuta-1,3-dien-2-yl acetate is used as a flavoring agent in the food industry due to its fruity odor. It adds a pleasant aroma and taste to various food products, enhancing their overall sensory experience.
Used in Fragrance Industry:
In the fragrance industry, 3-Methylbuta-1,3-dien-2-yl acetate is used as a component in creating various scents. Its fruity aroma contributes to the development of unique and appealing fragrances for perfumes, cosmetics, and other scented products.
Used in Chemical Synthesis:
3-Methylbuta-1,3-dien-2-yl acetate serves as a starting material or intermediate in the synthesis of various organic compounds. Its reactive double bonds and acetate group make it a versatile building block for the production of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Research and Development:
In the field of research and development, 3-Methylbuta-1,3-dien-2-yl acetate is utilized as a model compound for studying reactions and mechanisms involving isoprene derivatives. It helps scientists understand the behavior of similar compounds and develop new synthetic routes and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 16824-14-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,2 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16824-14:
(7*1)+(6*6)+(5*8)+(4*2)+(3*4)+(2*1)+(1*4)=109
109 % 10 = 9
So 16824-14-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O2/c1-5(2)6(3)9-7(4)8/h1,3H2,2,4H3
16824-14-9Relevant articles and documents
Ruthenium-Catalyzed Selective Addition of Carboxylic Acids to Alkynes.A Novel Synthesis of Enol Esters
Mitsudo, Take-aki,Hori, Yoji,Yamakawa, Yasushi,Watanabe, Yoshihisa
, p. 2230 - 2239 (2007/10/02)
Carboxylic acids react with alkynes in the presence of a catalytic amount of bis(ν5-cyclooctadienyl)ruthenium/trialkylphosphine/maleic anhydride in toluene at 60-80 deg.C to give enol esters having a terminal methylene group in good to excellent yields with high regioselectivity.The deuterium distributions in the products of the reaction of acetic acid-d with 1-hexyne and ethyl propargyl carbonate were examined.Kinetic measurments revealed that the rate has first-order dependence on carboxylic acid, alkyne, and the initial concentration of the ruthenium catalyst.
