6293-37-4 Usage
Description
2-Ethylhexyl propionate, also known as 2-ethylhexyl propionate, is a synthetic ester compound with the chemical formula C11H22O2. It is a colorless liquid with a fruity, apple-like odor and is soluble in organic solvents. It is commonly used in the study of oxidative degradation of synthetic esters and in the synthesis of perfumes.
Uses
Used in Chemical Research:
2-Ethylhexyl propionate is used as a model compound in chemical research for studying the oxidative degradation of synthetic esters. This helps in understanding the mechanisms and factors affecting the stability and degradation of synthetic esters, which is important for their applications in various industries.
Used in Perfumery Industry:
2-Ethylhexyl propionate is used as a fragrance ingredient in the perfumery industry. Its fruity, apple-like odor makes it a valuable component in creating various perfumes and fragrances. It contributes to the overall scent profile and helps in achieving the desired olfactory effect.
Used in Synthesis of Perfumes:
2-Ethylhexyl propionate is used as a raw material in the synthesis of perfumes. It can be combined with other fragrance ingredients to create unique and complex scent profiles. Its use in perfume synthesis allows for the development of new and innovative fragrances that cater to the diverse preferences of consumers.
Check Digit Verification of cas no
The CAS Registry Mumber 6293-37-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6293-37:
(6*6)+(5*2)+(4*9)+(3*3)+(2*3)+(1*7)=104
104 % 10 = 4
So 6293-37-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H22O2/c1-4-7-8-10(5-2)9-13-11(12)6-3/h10H,4-9H2,1-3H3
6293-37-4Relevant articles and documents
Reduction of Activated Alkenes by PIII/PV Redox Cycling Catalysis
Longwitz, Lars,Werner, Thomas
supporting information, p. 2760 - 2763 (2020/02/05)
The carbon–carbon double bond of unsaturated carbonyl compounds was readily reduced by using a phosphetane oxide catalyst in the presence of a simple organosilane as the terminal reductant and water as the hydrogen source. Quantitative hydrogenation was observed when 1.0 mol % of a methyl-substituted phosphetane oxide was employed as the catalyst. The procedure is highly selective towards activated double bonds, tolerating a variety of functional groups that are usually prone to reduction. In total, 25 alkenes and two alkynes were hydrogenated to the corresponding alkanes in excellent yields of up to 99 %. Notably, less active poly(methylhydrosiloxane) could also be utilized as the terminal reductant. Mechanistic investigations revealed the phosphane as the catalyst resting state and a protonation/deprotonation sequence as the crucial step in the catalytic cycle.
SYNTHESIS OF γ-KETOPIMELIC ACID DERIVATIVES BY RHODIUM CARBONYL-CATALYZED HYDROCARBONYLATION OF ACRYLIC ACID DERIVATIVES
Hong, Pangbu,Mise, Takaya,Yamazaki, Hiroshi
, p. 361 - 364 (2007/10/02)
The rhodium carbonyl-catalyzed reactions of acrylic acid derivatives (1) with CO in iso-propanol gave selectively γ-ketopimelic acid derivatives (2) in good yields.In the reaction of ethyl acrylate (1b) in iso-propanol-d8, deuterium scrambling in the methylene groups of the products (2b) was observed.
