600144-08-9 Usage
Uses
Used in Perfume Industry:
2,4-Heptadienoic acid, 7-phenyl-, methyl ester, (2E,4E)is used as a fragrance ingredient for its strong fruity and floral scent. It contributes to the creation of various perfume compositions, enhancing their overall aroma and appeal.
Used in Food Industry:
In the food industry, 2,4-Heptadienoic acid, 7-phenyl-, methyl ester, (2E,4E)is used as a flavoring agent. Its distinct fruity and floral notes add depth and complexity to a wide range of food and beverage products, improving their taste and consumer experience.
Used in Pharmaceutical Industry:
2,4-Heptadienoic acid, 7-phenyl-, methyl ester, (2E,4E)is used as an intermediate in the synthesis of other compounds, which may have potential applications in drug development. Its chemical properties make it a valuable building block for creating new pharmaceutical products.
Used in Chemical Synthesis:
2,4-Heptadienoic acid, 7-phenyl-, methyl ester, (2E,4E)is used as a chemical intermediate for the synthesis of various compounds. Its unique structure allows for further chemical reactions and modifications, making it a versatile component in the development of new chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 600144-08-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,0,1,4 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 600144-08:
(8*6)+(7*0)+(6*0)+(5*1)+(4*4)+(3*4)+(2*0)+(1*8)=89
89 % 10 = 9
So 600144-08-9 is a valid CAS Registry Number.
600144-08-9Relevant academic research and scientific papers
Enantioselective and Diastereodivergent Synthesis of Spiroindolenines via Chiral Phosphoric Acid-Catalyzed Cycloaddition
Gandon, Vincent,Masson, Géraldine,Mati?i?, Mateja,Neuville, Luc,Van Elslande, Elsa,Varlet, Thomas
supporting information, p. 11611 - 11619 (2021/08/16)
A diastereodivergent and enantioselective synthesis of chiral spirocyclohexyl-indolenines with four contiguous stereogenic centers is achieved by a chiral phosphoric acid-catalyzed cycloaddition of 2-susbtituted 3-indolylmethanols with 1,3-dienecarbamates. Modular access to two different diastereoisomers with high enantioselectivities was obtained by careful choice of reaction conditions. Their functional group manipulation provides an efficient access to enantioenriched spirocyclohexyl-indolines and -oxindoles. The origins of this stereocontrol have been identified using DFT calculations, which reveal an unexpected mechanism compared to our previous work dealing with enecarbamates.
Intramolecular Friedel-Crafts type reaction of vinyloxiranes linked to an ester group
Nagumo, Shinji,Miura, Toshie,Mizukami, Megumi,Miyoshi, Irie,Imai, Masanori,Kawahara, Norio,Akita, Hiroyuki
experimental part, p. 9884 - 9896 (2010/01/16)
The 7-endo Friedel-Crafts cyclization of arylpropyl vinyloxiranes was found to proceed regio- and stereoselectively to afford polyfunctional seven-membered carbocycles in excellent yields.
