61229-09-2 Usage
Description
(4E)-N-(4-hydroxy-3-methoxybenzyl)-6-methylhept-4-enamide is a chemical compound that belongs to the class of amides. It features a long carbon chain with a double bond and a methyl group, as well as a phenolic ring with a hydroxy and methoxy group attached. (4E)-N-(4-hydroxy-3-methoxybenzyl)-6-methylhept-4-enamide may exhibit potential biological activity due to its structural features, and it could be utilized in various fields such as pharmaceuticals, agrochemicals, or materials science. Further studies and research are required to explore its properties and potential applications.
Uses
Used in Pharmaceutical Industry:
(4E)-N-(4-hydroxy-3-methoxybenzyl)-6-methylhept-4-enamide is used as a potential pharmaceutical agent for its possible biological activity. Its unique structure may contribute to therapeutic effects, and ongoing research could reveal its efficacy in treating specific conditions or diseases.
Used in Agrochemical Industry:
In the agrochemical sector, (4E)-N-(4-hydroxy-3-methoxybenzyl)-6-methylhept-4-enamide may be employed as a component in the development of pesticides or herbicides. Its chemical properties could offer novel mechanisms for controlling pests or unwanted plant growth.
Used in Materials Science:
(4E)-N-(4-hydroxy-3-methoxybenzyl)-6-methylhept-4-enamide could be utilized in materials science for the creation of new materials with unique properties. Its structural components may contribute to the development of advanced materials with applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 61229-09-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,2 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61229-09:
(7*6)+(6*1)+(5*2)+(4*2)+(3*9)+(2*0)+(1*9)=102
102 % 10 = 2
So 61229-09-2 is a valid CAS Registry Number.
61229-09-2Relevant 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.
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.