6460-63-5 Usage
Uses
Used in Food and Beverage Industry:
(2E,4E,6E)-7-phenylhepta-2,4,6-trienal is used as a flavoring agent for its distinctive pungent and spicy aroma, enhancing the taste and aroma of various food and beverage products.
Used in Perfume Industry:
In the perfume industry, (2E,4E,6E)-7-phenylhepta-2,4,6-trienal is utilized as a fragrance component due to its appealing smell, contributing to the creation of various scented products.
Used in Pharmaceutical Applications:
(2E,4E,6E)-7-phenylhepta-2,4,6-trienal is considered for its potential medicinal uses, such as an anti-inflammatory, antioxidant, and anti-cancer agent, indicating its possible application in the development of therapeutic agents.
Used in Cosmetic and Personal Care Products:
Due to its pleasant aroma, (2E,4E,6E)-7-phenylhepta-2,4,6-trienal is also used in the production of perfumes, soaps, and other scented personal care products, adding a desirable fragrance to these items.
Check Digit Verification of cas no
The CAS Registry Mumber 6460-63-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,6 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6460-63:
(6*6)+(5*4)+(4*6)+(3*0)+(2*6)+(1*3)=95
95 % 10 = 5
So 6460-63-5 is a valid CAS Registry Number.
6460-63-5Relevant academic research and scientific papers
New Functionalized Horner-Wadsworth-Emmons Reagents: Useful Building Blocks in the Synthesis of Polyunsaturated Aldehydes. A Short Synthesis of (+/-)-(E,E)-Coriolic Acid
Kann, Nina,Rein, Tobias,Akermark, Bjoern,Helquist, Paul
, p. 5312 - 5323 (2007/10/02)
The new Horner-Wadsworth-Emmons reagents 4 and 5 transform carbonyl compounds into 2,4-pentadienals and 3-methyl-2,4-pentadienals, respectively.Reagent 4 gives good yields of the desired products with a variety of aldehydes and ketones; reagent 5 generally gives good yields with aldehydes, but gives lower yields with ketones.The reactions proceed under mild conditions and give the products as predominantly 2E,4E isomers, with moderate to good stereoselectivity.In general, pure samples of the 2E,4E-dienals can be obtained after chromatography.Reagents 4 have been used in the key step in a short synthesis of (+/-)-13-hydroxy-9(E),11(E)-octadecanoic acid ((E,E)-coriolic aicd, 45).
