71240-51-2 Usage
Description
6-Decenamide,N-[(4-hydroxy-3-methoxyphenyl) methyl]-8-methyl-,(6E)is a chemical compound belonging to the amide family, characterized by a long-chain structure with a methyl substituent at the 8th carbon and a hydroxy-methoxyphenyl methyl group at the N-position. 6-Decenamide,N-[(4-hydroxy-3-methoxyphenyl) methyl]-8-methyl-,(6E) features a double bond at the 6th position and has potential applications in various industries.
Uses
Used in Fragrance and Flavoring Industry:
6-Decenamide,N-[(4-hydroxy-3-methoxyphenyl) methyl]-8-methyl-,(6E)is used as a fragrance and flavoring agent due to its unique scent and taste properties. It can be incorporated into various products to enhance their sensory appeal.
Used in Pharmaceutical Industry:
6-Decenamide,N-[(4-hydroxy-3-methoxyphenyl) methyl]-8-methyl-,(6E)is used as an active pharmaceutical ingredient or as a component in the formulation of medications. Its specific properties may contribute to the development of new drugs or the improvement of existing ones.
Used in Cosmetic Industry:
6-Decenamide,N-[(4-hydroxy-3-methoxyphenyl) methyl]-8-methyl-,(6E)is used as a cosmetic ingredient for its potential benefits in skincare and personal care products. It may be incorporated into creams, lotions, or other formulations to provide specific effects or improvements to the product's performance.
It is crucial to handle 6-Decenamide,N-[(4-hydroxy-3-methoxyphenyl) methyl]-8-methyl-,(6E)with care and adhere to safety guidelines when working with this compound in any of the mentioned applications.
Check Digit Verification of cas no
The CAS Registry Mumber 71240-51-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,2,4 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 71240-51:
(7*7)+(6*1)+(5*2)+(4*4)+(3*0)+(2*5)+(1*1)=92
92 % 10 = 2
So 71240-51-2 is a valid CAS Registry Number.
71240-51-2Relevant articles and documents
A general and stereoselective synthesis of the capsaicinoids via the orthoester Claisen rearrangement
Kaga, Harumi,Goto, Kouhei,Takahashi, Tomiki,Hino, Masao,Tokuhashi, Takashi,Orito, Kazuhiko
, p. 8451 - 8470 (2007/10/03)
Capsaicin, a main pungent principle of hot pepper, and its 15 analogs have been efficiently synthesized. The key step of this synthetic scheme is the orthoester Claisen rearrangement, which transformed allylic alcohols 2A-C to (E)-alkenoates 3A-C (E/Z > 100) in a highly stereoselective manner. The subsequent carbon chain elongations on 3 based on the cyanation or the malonic acid ester synthesis afforded (E)-alkenoic acids 8, which were converted to the corresponding acid chloride and then coupled with vanillylamine to give capsaicinoids. HPLC and CE (capillary electrophoresis) analyses of these capsaicinoids were also carried out.
