77448-63-6 Usage
Uses
Used in Pharmaceutical Industry:
DODECA-2,4,8,10-TETRAENOIC ACID ISOBUTYLAMIDE is used as an active compound for its potential therapeutic effects. As the major constituent in human blood plasma after Echinacea purpurea consumption, it may contribute to the plant's immunomodulatory, anti-inflammatory, and antiviral properties, making it a promising candidate for further pharmaceutical research and development.
Used in Herbal Medicine:
DODECA-2,4,8,10-TETRAENOIC ACID ISOBUTYLAMIDE is used as a key ingredient in herbal medicine for its potential to support the immune system. Echinacea purpurea has been traditionally used to prevent and treat colds, flu, and other infections, and DODECA-2,4,8,10-TETRAENOIC ACID ISOBUTYLAMIDE may play a role in those beneficial effects.
Used in Nutritional Supplements:
DODECA-2,4,8,10-TETRAENOIC ACID ISOBUTYLAMIDE can be used as an ingredient in nutritional supplements, particularly those aimed at enhancing immune function and overall well-being. Its presence in human blood plasma after Echinacea purpurea consumption suggests that it may be a bioavailable and effective component for immune support.
Check Digit Verification of cas no
The CAS Registry Mumber 77448-63-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,4,4 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 77448-63:
(7*7)+(6*7)+(5*4)+(4*4)+(3*8)+(2*6)+(1*3)=166
166 % 10 = 6
So 77448-63-6 is a valid CAS Registry Number.
77448-63-6Relevant academic research and scientific papers
Polyunsaturated alkyl amides from echinacea: Synthesis of diynes, enynes, and dienes
Matovic, Nicholas J.,Hayes, Patricia Y.,Penman, Kerry,Lehmann, Reginald P.,De Voss, James J.
, p. 4467 - 4481 (2011/07/30)
The synthesis of 20 alkyl amides, including 15 naturally occurring polyunsaturated alkyl amides previously identified from Echinacea spp. (1-13 and 62) or from Achilla sp. (55) and five previously unknown geometric isomers (23, 28, 67, 73, and 80), is described. Importantly, these amides include all of the major alkyl amides present in commercially used Echinacea extracts. The syntheses demonstrate methodology used for constructing alkyl amides containing conjugated diyne and isomerically pure enyne and diene moieties and may be adapted easily for the preparation of other alkyl amides present in Echinacea spp. Terminal-conjugated diynes were prepared by a Cadiot-Chodkiewitz coupling/deprotection sequence utilizing a protected bromoacetylene, and methyl-substituted diynes were made via a base-catalyzed rearrangement of terminal-skipped diynes. Conjugated dienes were prepared conveniently and with high stereoselectivity by the reduction of enynes or diynes with Rieke zinc. With the exception of 1-2 and 11-12, the alkyl amides are synthesized here for the first time, and their NMR data are consistent with that of the reported isolated natural compounds.
