58493-48-4 Usage
Description
(7E)-N-(4-hydroxy-3-methoxybenzyl)-9-methyldec-7-enamide is a chemical compound with potential pharmaceutical and medicinal properties. It features a long hydrocarbon chain with a double bond and a terminal amide group. The presence of hydroxyl and methoxy groups on the benzene ring indicates possible antioxidant and anti-inflammatory characteristics. Additionally, the amide functional group suggests its potential use as a pain reliever or analgesic. (7E)-N-(4-hydroxy-3-methoxybenzyl)-9-methyldec-7-enamide may be valuable in the development of drugs for treating pain and inflammation.
Uses
Used in Pharmaceutical Industry:
(7E)-N-(4-hydroxy-3-methoxybenzyl)-9-methyldec-7-enamide is used as a potential therapeutic agent for its antioxidant and anti-inflammatory properties, which can be beneficial in the treatment of various conditions characterized by inflammation and oxidative stress.
Used in Pain Management:
In the pharmaceutical industry, (7E)-N-(4-hydroxy-3-methoxybenzyl)-9-methyldec-7-enamide is used as a potential analgesic for its pain-relieving properties, making it a candidate for the development of drugs aimed at managing pain.
Used in Anti-Inflammatory Applications:
(7E)-N-(4-hydroxy-3-methoxybenzyl)-9-methyldec-7-enamide is also used as an anti-inflammatory agent due to its potential to reduce inflammation, which can be useful in the treatment of conditions like arthritis and other inflammatory diseases.
Used in Antioxidant Formulations:
(7E)-N-(4-hydroxy-3-methoxybenzyl)-9-methyldec-7-enamide can be utilized as an antioxidant in the development of medications or supplements designed to combat oxidative stress and related diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 58493-48-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,4,9 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 58493-48:
(7*5)+(6*8)+(5*4)+(4*9)+(3*3)+(2*4)+(1*8)=164
164 % 10 = 4
So 58493-48-4 is a valid CAS Registry Number.
58493-48-4Relevant 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.
The Capsaicinoids: Their Separation, Synthesis, and Mutagenicity
Gannett, Peter M.,Nagel, Donald L.,Reilly, Pam J.,Lawson, Terence,Sharpe, Jody,Toth, Bela
, p. 1064 - 1071 (2007/10/02)
Capsaicin (1b), the pungent ingredient in many varietes of Capsicums has recently been implicated as a possible carcinogen.When obtained from natural sources 1b is always accompanied by a number of related homologues.We have isolated seven of these homologues, characterized them, and synthesized them by a general and unique route developed in our laboratories.Also reported are mutagenicity data for 1b and an extract of red pepper as measured by the Ames assay and the V-79 mammalian cell assay.
