72894-15-6 Usage
Uses
Used in Food and Beverage Industry:
Trideca-2,12-dienal is used as a flavoring agent for imparting a green, citrus-like scent often found in fruits and essential oils.
Used in Perfumes and Personal Care Products:
Trideca-2,12-dienal is used as a fragrance ingredient to provide a fresh and natural aroma.
Used in Pharmaceutical and Nutraceutical Industry:
Trideca-2,12-dienal has been studied for its potential biological activities, including anti-inflammatory and antioxidant properties, making it a candidate for use in pharmaceutical and nutraceutical applications.
It is important to handle trideca-2,12-dienal with caution, as it may cause skin and eye irritation in high concentrations.
Check Digit Verification of cas no
The CAS Registry Mumber 72894-15-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,8,9 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 72894-15:
(7*7)+(6*2)+(5*8)+(4*9)+(3*4)+(2*1)+(1*5)=156
156 % 10 = 6
So 72894-15-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H22O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14/h2,11-13H,1,3-10H2/b12-11+
72894-15-6Relevant articles and documents
Cumulated Ylides, XII. A Stereoselective Synthetic Method for (Z)-α,β-Unsaturated Aldehydes
Bestmann, Hans Juergen,Roth, Kurt,Ettlinger, Manfred
, p. 161 - 171 (2007/10/02)
(2-Ethoxyvinyl)triphenylphosphonium bromide (5) is converted with sodium amide into the corresponding phosphaallenylide 6 which adds ethanol forming the ylide 7. 7 is also obtained by the reaction of 5 with sodium ethanolate.The Wittig reaction of 7 with aldehydes 2 proceeds with high (Z)-stereoselectivity to give (Z)-α,β-unsaturated acetals 8 which are cleaved under well defined conditions with p-toluenesulfonic acid or with wet silica gel to (Z)-α,β-unsaturated aldehydes 9.
