221671-41-6 Usage
Uses
Used in Pharmaceutical Research:
(S)-3-(Benzoyloxy)quinuclidine is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and chirality allow for the creation of novel drugs with specific therapeutic properties.
Used in the Treatment of Alzheimer's Disease:
(S)-3-(Benzoyloxy)quinuclidine is used as an acetylcholinesterase inhibitor for the potential treatment of Alzheimer's disease. By inhibiting the enzyme acetylcholinesterase, it may help improve cognitive function and slow the progression of the disease.
Used in Asymmetric Organic Reactions:
(S)-3-(Benzoyloxy)quinuclidine is used as a catalyst in asymmetric organic reactions, which are crucial for the synthesis of enantiomerically pure compounds. Its application in this field can lead to the development of more efficient and selective synthetic routes for pharmaceuticals and other specialty chemicals.
Used in Organic Synthesis:
(S)-3-(Benzoyloxy)quinuclidine is used as a building block in the preparation of complex organic molecules, particularly those with potential applications in the pharmaceutical industry. Its versatility and reactivity make it a valuable compound for the synthesis of a wide range of target molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 221671-41-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,1,6,7 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 221671-41:
(8*2)+(7*2)+(6*1)+(5*6)+(4*7)+(3*1)+(2*4)+(1*1)=106
106 % 10 = 6
So 221671-41-6 is a valid CAS Registry Number.
221671-41-6Relevant academic research and scientific papers
Simple one-pot process for the bioresolution of tertiary amino ester protic ionic liquids using subtilisin
Brossat, Maude,Moody, Thomas S.,Taylor, Stephen J.C.,Wiffen, Jonathan W.
experimental part, p. 2112 - 2116 (2010/02/28)
An efficient hydrolase-catalyzed bioresolution of tertiary amino ester protic ionic liquids has been demonstrated. Protic ionic liquids have been prepared in one step from the corresponding tertiary amino alcohols by treatment with butyric anhydride. Afte
Interactions of chiral quinuclidin-3-yl benzoates with butyrylcholinesterase: Kinetic study and docking simulations
Primozic, Ines,Hrenar, Tomica,Tomic, Srdanka,Meic, Zlatko
, p. 608 - 614 (2007/10/03)
Both enantiomers of quinuclidin-3-yl benzoate (RQBz and SQBz) were synthesized in order to examine the stereoselectivity of the hydrolysis of these esters catalyzed by horse serum butyrylcholinesterase (BChE). The hydrolysis of benzoylcholine (BzCh) was a
