22932-25-8 Usage
Uses
As the provided materials do not specify any particular applications for (1β,5β)-8-Methyl-3β-phenyl-8-azabicyclo[3.2.1]octan-3α-ol, it is not possible to list its uses based on the information given. However, given its classification as a chemical compound with a unique structure, it may be used in various industries once its properties and potential uses are better understood through further research. Possible applications could include pharmaceutical development, as an intermediate in chemical synthesis, or in other specialized fields where its specific molecular structure could be advantageous.
Check Digit Verification of cas no
The CAS Registry Mumber 22932-25-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,3 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22932-25:
(7*2)+(6*2)+(5*9)+(4*3)+(3*2)+(2*2)+(1*5)=98
98 % 10 = 8
So 22932-25-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H19NO/c1-15-12-7-8-13(15)10-14(16,9-12)11-5-3-2-4-6-11/h2-6,12-13,16H,7-10H2,1H3
22932-25-8Relevant academic research and scientific papers
The discovery of tropane derivatives as nociceptin receptor ligands for the management of cough and anxiety
Ho, Ginny D.,Anthes, John,Bercovici, Ana,Caldwell, John P.,Cheng, Kuo-Chi,Cui, Xiaoming,Fawzi, Ahmad,Fernandez, Xiomara,Greenlee, William J.,Hey, John,Korfmacher, Walter,Lu, Sherry X.,McLeod, Robbie L.,Ng, Fay,Torhan, April Smith,Tan, Zheng,Tulshian, Deen,Varty, Geoffrey B.,Xu, Xiaoying,Zhang, Hongtao
scheme or table, p. 2519 - 2523 (2009/12/25)
The discovery of 1 as a high-affinity ligand for the nociceptin receptor has led to the synthesis of a series of tropane (8-methyl-8-azabicyclo[3.2.1]octane) derivatives as optimized ligands. These compounds exhibit high affinity for the nociceptin recept
Opioid properties of some derivatives of pethidine based on tropane
Casy,Dewar,Pascoe
, p. 787 - 790 (2007/10/02)
The preparation of some tropane analogues of pethidine and its reversed ester, chiefly with preferred 3α-m-hydroxyphenyl chair conformations, is described. The former were secured from tropan-3-one in a sequence of reactions involving cyanide attack, hydr
