16824-14-9 Usage
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 academic research and scientific papers
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.
Process for the preparation of unsaturated ketones
-
, (2008/06/13)
Ketones, which are intermediates in the synthesis of vitamin A or perfumes, and have the general formula: EQU1 wherein R1 is hydrogen or C1-10 hydrocarbon, R2 and R3 are hydrogen or C1-4 alkyl, R4 and R5 are hydrogen or together form a --CH2 --CH2 --C(CH3)2 -- group, R6 and R7 are hydrogen or C1-10 hydrocarbon, or together with the carbon atom to which they are joined form a hydrocarbon ring of up to 10 carbons, or EQU2 forms a hydrocarbon ring of up to 10 carbons joined through R6 and R8 or R7 and R8, R8 is hydrogen or C1-10 hydrocarbon and n is 0-6, are prepared by reacting an unsaturated halide of formula EQU3 wherein X is halogen, with an enol ester of formula EQU4 wherein R9 is C1-20 hydrocarbon, in the presence of a metal catalyst.
