529-80-6 Usage
Uses
Used in Pharmaceutical Industry:
Multiflorine is used as a pharmaceutical compound for its potential therapeutic effects. Multiflorine has been found to exhibit various biological activities, such as anti-inflammatory, analgesic, and anti-cancer properties, which make it a promising candidate for the development of new drugs and treatments.
Used in Cosmetic Industry:
Multiflorine is used as an active ingredient in the cosmetic industry for its potential skin care benefits. Multiflorine may have antioxidant, anti-aging, and skin-soothing properties, which can be utilized in the formulation of skincare products to improve skin health and appearance.
Used in Agricultural Industry:
Multiflorine is used as a natural pesticide in the agricultural industry due to its potential insecticidal and antifungal properties. Multiflorine can be employed as a part of integrated pest management strategies to control pests and diseases in crops, reducing the reliance on synthetic chemicals and promoting sustainable agriculture.
Used in Food Industry:
Multiflorine is used as a natural additive in the food industry for its potential preservative and flavor-enhancing properties. Multiflorine may help extend the shelf life of food products and improve their taste and aroma, making it a valuable ingredient in the development of new food products.
Check Digit Verification of cas no
The CAS Registry Mumber 529-80-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 529-80:
(5*5)+(4*2)+(3*9)+(2*8)+(1*0)=76
76 % 10 = 6
So 529-80-6 is a valid CAS Registry Number.
InChI:InChI=1/C15H22N2O/c18-13-4-6-17-9-11-7-12(15(17)8-13)10-16-5-2-1-3-14(11)16/h4,6,11-12,14-15H,1-3,5,7-10H2/t11-,12+,14-,15+/m0/s1
529-80-6Relevant academic research and scientific papers
The stereochemistry of the reduction of cyclic enaminones
Wysocka,Przybyl
, p. 973 - 984 (2007/10/03)
The stereo- and regiochemistry of di-, tri-, and tetracyclic enaminones upon catalytic hydrogenation on Pd and Pt catalysts seems to be mainly a function of the catalyst and the medium. The highest stereoselectivity was observed for multiflorine on Pd/C in which 99% of equatorial alcohol were formed in this case, the formation of alcohols proceeds via a ketonic intermediate. On platinum, irrespective of the solvent used (EtOH, H2O, AcOH, HCl), the hydrogenation reaction proceeds through ketonic (piperidone system) and dehydro (pyridone system) intermediates. In EtOH or H2O solution, the dehydro product remains unchanged, whereas the ketonic intermediate is reduced to a mixture of epimeric alcohols. In HCl and acetic acid, both intermediates are hydrogenolyzed to a product with a methylene group, but the ketonic one is additionally reduced to a mixture of epimeric alcohols. Reductions with complex metal hydrides provide mixtures of epimeric alcohols with a predominance of equatorial orientation. The structures of products were determined by NMR spectroscopy and/or by GC-MS analysis.
STEREOSTRUCTURE OF (-)-MULTIFLORINE N-OXIDE: A NEW LUPIN ALKALOID FROM LUPINUS HIRSUTUS
Takamatsu, Satoshi,Saito, Kazuki,Ohmiya, Shigeru,Murakoshi, Isamu
, p. 1167 - 1171 (2007/10/02)
A new lupin alkaloid, (-)-multiflorine N-oxide (1) was isolated from the seedlings of Lupinus hirsutus together with twelve known alkaloids.The structure of 1 was determined by spectroscopic methods and by chemical transformations.
