56767-18-1 Usage
Uses
Used in Fragrance Industry:
(2E,6E)-2,6-Octadienal is used as a fragrance ingredient for its strong, sweet, floral scent. It is incorporated into perfumes and other scented products to provide a pleasant and natural aroma.
Used in Flavor Industry:
(2E,6E)-2,6-Octadienal is used as a flavoring agent in the food industry. Its natural, sweet, and floral taste profile makes it suitable for enhancing the flavor of various food products, particularly those that aim to mimic the taste of certain fruits or flowers.
Used in Cosmetics and Personal Care Products:
(2E,6E)-2,6-Octadienal is used as a scent component in cosmetics and personal care products. Its pleasant and natural aroma adds to the sensory experience of these products, making them more appealing to consumers.
Used in Aromatherapy:
(2E,6E)-2,6-Octadienal can be used in aromatherapy for its calming and soothing properties. Its sweet and floral scent can help create a relaxing atmosphere and promote a sense of well-being.
Used in the Production of Essential Oils:
(2E,6E)-2,6-Octadienal can be used in the production of essential oils, which are often used in various applications such as aromatherapy, massage, and skincare. Its strong, sweet, and floral scent can contribute to the overall aroma and therapeutic properties of these essential oils.
Check Digit Verification of cas no
The CAS Registry Mumber 56767-18-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,7,6 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 56767-18:
(7*5)+(6*6)+(5*7)+(4*6)+(3*7)+(2*1)+(1*8)=161
161 % 10 = 1
So 56767-18-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O/c1-2-3-4-5-6-7-8-9/h2-3,6-8H,4-5H2,1H3/b3-2+,7-6+
56767-18-1Relevant academic research and scientific papers
Endo-oxacyclizations of polyepoxides: Biomimetic synthesis of fused polycyclic ethers
McDonald, Frank E.,Bravo, Fernando,Wang, Xia,Wei, Xudong,Toganoh, Motoki,Rodriguez, J. Ramon,Do, Bao,Neiwert, Wade A.,Hardcastle, Kenneth I.
, p. 2515 - 2523 (2007/10/03)
Boron trifluoride-etherate promotes the endo-selective oxacyclization of polyepoxides derived from various acyclic terpenoid polyalkenes, including geraniol, farnesol, and geranylgeraniol, providing an efficient and stereoselective synthesis of substituted oxepanes and fused polyoxepanes. The mechanism of the oxacyclization reaction probably involves intramolecular nucleophilic addition of epoxide oxygen to open another epoxide that is activated as an electrophile by the Lewis acid. These oxacyclizations proceed stereospecifically with inversion of configuration upon opening of each epoxide to provide trans-fused polycyclic products. The oxacyclization cascade is terminated by a tethered nucleophile, which may be the carbonyl oxygen of a ketone, ester, or carbonate, or a trisubstituted alkene. The best oxacyclization yields are generally observed with tert-butyl carbonate as the terminating nucleophile, although in some cases the oxacyclization products include formation of tert-butyl ethers as a minor product. The oxacyclization transformations described herein may mimic ring-forming steps in the biosynthesis of trans-syn-trans-fused polycyclic ether marine natural products.
A SIMPLE CONVERSION OF N,N-DIMETHYL-2-ALKENYLAMINE TO 2-ALKENAL
Takabe, Kunihiko,Yamada, Takashi,Katagiri, Takao
, p. 1987 - 1988 (2007/10/02)
Treatment of N,N-dimethyl-2-alkenylamine with 30percent H2O2 followed by acetic anhydride affords 2-alkenal (α,β-unsaturated aldehyde) in good isolated yield.
