5462-94-2 Usage
Description
(2E,4E,6E,8E,10E)-11-phenylundeca-2,4,6,8,10-pentaenal is an unsaturated aldehyde with a complex molecular structure that features multiple double bonds in its carbon chain and a six-carbon aromatic ring due to the presence of a phenyl group. This unique structure and reactivity make it valuable in various chemical applications.
Uses
Used in Organic Synthesis:
(2E,4E,6E,8E,10E)-11-phenylundeca-2,4,6,8,10-pentaenal is used as a key intermediate in organic synthesis for the production of various compounds.
Used in Fragrance Industry:
In the fragrance industry, (2E,4E,6E,8E,10E)-11-phenylundeca-2,4,6,8,10-pentaenal is used as a building block for creating complex and unique scents due to its reactive aldehyde functional group.
Used in Pharmaceutical Industry:
(2E,4E,6E,8E,10E)-11-phenylundeca-2,4,6,8,10-pentaenal is used as a starting material or intermediate in the synthesis of pharmaceuticals, taking advantage of its unique structure and reactivity to produce novel drug candidates.
Used in Fine Chemicals Production:
(2E,4E,6E,8E,10E)-11-phenylundeca-2,4,6,8,10-pentaenal is utilized in the production of fine chemicals, where its specific molecular structure and properties are harnessed for specialized applications.
Check Digit Verification of cas no
The CAS Registry Mumber 5462-94-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5462-94:
(6*5)+(5*4)+(4*6)+(3*2)+(2*9)+(1*4)=102
102 % 10 = 2
So 5462-94-2 is a valid CAS Registry Number.
5462-94-2Relevant articles and documents
Stereoselective organocatalytic oxidation of alcohols to enals: A homologation method to prepare polyenes
Chen, Xiaobei,Zhang, Yinan,Wan, Huixin,Wang, Wei,Zhang, Shilei
, p. 3532 - 3535 (2016/03/04)
A novel method for organocatalytic oxidation through oxidative enamine catalysis was developed with excellent compatibility for the direct syntheses of enals from simple saturated alcohols. By using this amine-catalyzed IBX-oxidation, a wide range of aromatic and aliphatic substituted enals were successfully generated in high yields and exclusively stereoselective E-geometry. Moreover, varying the solvents and/or the loading amounts of IBX allowed for the selective oxidation of alcohols and aldehydes. Importantly, the homologous application of this method provided a selective and efficient way of preparing various highly sensitive conjugated polyene frameworks, which are enriched in natural products.