53398-76-8 Usage
Uses
Used in Food Industry:
2,4-Hexadienal is used as a flavoring agent for enhancing the taste and aroma of various food products, capitalizing on its naturally occurring presence in plants and fruits to provide a rich and authentic flavor profile.
Used in Cosmetic Industry:
In the cosmetic sector, 2,4-Hexadienal serves as a fragrance component, adding pleasant and evocative scents to products, leveraging its inherent aromatic properties found in nature.
Used in Perfumery:
2,4-Hexadienal is utilized in the production of perfumes, where its aromatic qualities contribute to the creation of complex and long-lasting fragrances.
Used as a Chemical Intermediate:
2,4-Hexadienal plays a crucial role as a chemical intermediate in the synthesis of other compounds, facilitating the development of a range of chemical products through its reactive aldehyde group.
Check Digit Verification of cas no
The CAS Registry Mumber 53398-76-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,9 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 53398-76:
(7*5)+(6*3)+(5*3)+(4*9)+(3*8)+(2*7)+(1*6)=148
148 % 10 = 8
So 53398-76-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H8O/c1-2-3-4-5-6-7/h2-6H,1H3/b3-2-,5-4+
53398-76-8Relevant academic research and scientific papers
Total synthesis of sperabillin A and C
Allmendinger, Lars,Bauschke, Gerd,Paintner, Franz F.
, p. 2615 - 2618 (2007/10/03)
The first total synthesis of sperabillin A and an improved total synthesis of sperabillin C have been achieved in 11 steps from N-Boc-Omethyl-L-tyrosine. The stereoselective pathway to the core (3R,5R)-3,6-diamino-5-hydroxyhexanoic acid involves an Arndt-
Palladium-Catalyzed Three Carbon Chain Extension Reactions with Acrolein Acetals. A Convenient Synthesis of Conjugated Dienals
Patel, Babu A.,Kim, Jin-Il I.,Bender, Diana D.,Kao, Lien-Chung,Heck, Richard F.
, p. 1061 - 1067 (2007/10/02)
A variety of vinylic halides has been found to react with acrolein or methacrolein acetals and amines with palladium catalysts to form 5-amino 3-enal acetals and/or dienal acetals.The reaction products yield 2,4-dienals on treatment with aqueous acids, in moderate to good yields.Crotonaldehyde dimethyl acetal also undergoes the reaction, but only in low yields. 3-Buten-2-one ethylene ketal reacted well under the same conditions, however, and Hofmann elimination and hydrolysis of the product amine gave (E,E)-3,5-heptadien-2-one in 90percent yield.
