5307-19-7 Usage
Uses
Used in Pharmaceutical Synthesis:
1-(alpha-pyridine)-2-propanol is used as a precursor in the pharmaceutical industry for the synthesis of various drugs. Its ability to chelate with metal ions and its compatibility with a range of chemical reactions make it an essential component in the development of new medications.
Used in Organic Synthesis:
In the realm of organic synthesis, 1-(alpha-pyridine)-2-propanol is utilized as a key intermediate. Its structural features facilitate its involvement in numerous chemical reactions, contributing to the formation of a wide array of organic compounds.
Used as a Chelating Agent:
1-(alpha-pyridine)-2-propanol is used as a chelating agent in various applications. Its capacity to form stable complexes with metal ions is particularly useful in stabilizing reactive species and controlling reaction conditions.
Used for Anti-Inflammatory and Anti-Cancer Properties:
1-(alpha-pyridine)-2-propanol has been studied for its potential anti-inflammatory and anti-cancer properties. Researchers are exploring its use in therapeutic applications, particularly in the development of treatments for inflammatory conditions and various types of cancer.
Used as a Solvent and Stabilizer in Industrial Processes:
1-(alpha-pyridine)-2-propanol also serves as a solvent and stabilizer in a range of industrial processes. Its ability to dissolve a variety of substances and stabilize formulations makes it a valuable asset in the manufacturing and processing sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 5307-19-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,0 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5307-19:
(6*5)+(5*3)+(4*0)+(3*7)+(2*1)+(1*9)=77
77 % 10 = 7
So 5307-19-7 is a valid CAS Registry Number.
5307-19-7Relevant academic research and scientific papers
NHC-stabilised Rh nanoparticles: Surface study and application in the catalytic hydrogenation of aromatic substrates
Martinez-Espinar, Francisco,Blondeau, Pascal,Nolis, Pau,Chaudret, Bruno,Claver, Carmen,Castillón, Sergio,Godard, Cyril
, p. 113 - 127 (2017/09/08)
New Rh-NPs stabilised by N-Heterocyclic Carbenes (NHC) were synthesized by decomposition of [Rh(η3-C3H5)3] under H2 atmosphere and fully characterized. Surface studies by FT-IR and NMR spectroscopy employing isotopically labelled ligands were also performed. The Rh0.2 NPs are active catalysts in the reduction of various aromatic substrates. In the reduction of phenol, high selectivities to cyclohexanone or cyclohexanol were obtained depending on the reaction conditions. However, this catalytic system exhibited much lower activity in the hydrogenation of substituted phenols. Pyridine was easily hydrogenated under mild conditions and interestingly, the hydrogenation of 4-methyl and 4-trifluoromethylpyridine resulted slower than that of 2-methylpyridine. The hydrogenation of 1-(pyridin-2-yl)propan-2-one provided the β-enaminone 13a in high yield as a consequence of the partial reduction of the pyridine ring followed by isomerization. Quinoline could be either partially hydrogenated to 1,2,3,4-tetrahydroquinoline or fully reduced to decahydroquinoline by adjusting the reaction conditions.
