77984-60-2 Usage
Uses
Used in Medicinal Chemistry and Drug Discovery:
Geranylgeranylamine is used as a precursor for the biosynthesis of various natural products, making it a valuable compound in the field of medicinal chemistry and drug discovery. Its unique structure and potential pharmacological activities may contribute to the development of new therapeutic agents.
Used in Antioxidant and Anti-Inflammatory Applications:
Geranylgeranylamine is used as an antioxidant and anti-inflammatory agent due to its potential biological activities. Further research is needed to fully understand its properties and potential applications in these fields.
Used in Cosmetics Industry:
Geranylgeranylamine may have potential applications in the cosmetics industry, where it can be used as an ingredient in skincare products for its antioxidant and anti-inflammatory properties.
Used in Nutraceutical Industry:
Geranylgeranylamine may also have potential applications in the nutraceutical industry, where it can be used as a dietary supplement for its potential health benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 77984-60-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,9,8 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 77984-60:
(7*7)+(6*7)+(5*9)+(4*8)+(3*4)+(2*6)+(1*0)=192
192 % 10 = 2
So 77984-60-2 is a valid CAS Registry Number.
77984-60-2Relevant academic research and scientific papers
Terpene Amine Synthesis via Palladium-Catalyzed Isoprene Telomerization with Ammonia
Keim, Wilhelm,Roeper, Michael
, p. 3702 - 3707 (2007/10/02)
Isoprene and dry ammonia could be converted in a catalytic process in good yields into a mixture of primary, secondary, and tertiary terpene amines.Homogeneous catalysts formed from palladium acetylacetonate and tributyl phosphite showed the best activities and selectivities for the telomerization.Seven amines were isolated as the main products from the reaction mixture and were characterized by their spectral data.Tail-to-tail coupling of the isoprene units was predominant though under certain conditions α-linalylamine, which shows a head-to-tail structure, prevailed.The product distribution could be controlled by cocatalysts and reaction parameters.The formation of primary terpene amines was favored by short reaction times and high ammonia/isoprene ratios.The proper choice of solvents and especially ligands is shown to be essential, and a strong dependence on the catalyst concentration was observed.A mechanism involving bridged binuclear palladium complexes as the active species is discussed.
