17244-79-0 Usage
General Description
1,2-diphenyl-2-(pyrrolidin-1-yl)ethanol is a chemical compound with the molecular formula C20H23NO. It is a chiral molecule, meaning it exists in two mirror image forms, and is commonly used as a precursor in the production of pharmaceuticals and other organic compounds. The compound is a white crystalline solid that is sparingly soluble in water and organic solvents. It is primarily used in the synthesis of various drugs, including analgesics, anticonvulsants, and antihistamines, due to its ability to modify the activity of certain neurotransmitter systems in the central nervous system. Additionally, it has shown potential as an anti-inflammatory and anti-cancer agent in some studies. However, as a chiral compound, its enantiomers may have different biological activities, making it important to consider the stereochemistry of the molecule in pharmaceutical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 17244-79-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,4 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17244-79:
(7*1)+(6*7)+(5*2)+(4*4)+(3*4)+(2*7)+(1*9)=110
110 % 10 = 0
So 17244-79-0 is a valid CAS Registry Number.
17244-79-0Relevant articles and documents
Hydrogen Bonding Phase-Transfer Catalysis with Potassium Fluoride: Enantioselective Synthesis of β-Fluoroamines
Pupo, Gabriele,Vicini, Anna Chiara,Ascough, David M. H.,Ibba, Francesco,Christensen, Kirsten E.,Thompson, Amber L.,Brown, John M.,Paton, Robert S.,Gouverneur, Véronique
supporting information, p. 2878 - 2883 (2019/02/14)
Potassium fluoride (KF) is an ideal reagent for fluorination because it is safe, easy to handle and low-cost. However, poor solubility in organic solvents coupled with limited strategies to control its reactivity has discouraged its use for asymmetric C-F
Towards phase-transfer catalysts with a chiral anion: Inducing asymmetry in the reactions of cations
Carter, Christabel,Fletcher, Sarah,Nelson, Adam
, p. 1995 - 2004 (2007/10/03)
The ability of chiral anions, for example bis[1,1′-bi-2-naphtholato]borate, to induce asymmetry in the reactions of prochiral cations was investigated. Ion-pairing of a borate anion with an aziridinium ion was demonstrated by NMR spectroscopy. The additio
