146747-65-1 Usage
General Description
N-Cbz-9-azabicyclo[3.3.1]nonan-3-one is a chemical compound which, like many chemicals, is identifiable by its specific structure and the arrangement of its atomic constituents. Its name might suggest that it has some relevancy to the fields of chemistry or materials science, although specific information about this compound is very scarce. The properties, applications, and even potential hazards of this compound are not commonly available. Like all chemicals, the use and handling of N-Cbz-9-azabicyclo[3.3.1]nonan-3-one would need to be conducted under certain safety precautions, with a strong understanding of its reactions with other elements or compounds. Detailed and accurate information about this chemical compound would need to be obtained from credible scientific resources or databases.
Check Digit Verification of cas no
The CAS Registry Mumber 146747-65-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,7,4 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 146747-65:
(8*1)+(7*4)+(6*6)+(5*7)+(4*4)+(3*7)+(2*6)+(1*5)=161
161 % 10 = 1
So 146747-65-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H19NO3/c18-15-9-13-7-4-8-14(10-15)17(13)16(19)20-11-12-5-2-1-3-6-12/h1-3,5-6,13-14H,4,7-11H2
146747-65-1Relevant articles and documents
Bicyclo[3.3.1]nonanes as synthetic intermediates. Part 19. Asymmetric cleavage of ω-azabicyclo[3.n.1]alkan-3-ones at the 'fork head'
Momose, Takefumi,Toshima, Minoru,Toyooka, Naoki,Hirai, Yoshiro,Eugster, Conrad Hans
, p. 1307 - 1313 (2007/10/03)
Asymmetric cleavage of ω-azabicyclo[3.n.1]alkan-3-ones was achieved by asymmetric deprotonation at the 'fork head' ketone system with Koga's chiral base and subsequent ozonolysis of the resulting chiral silyl enol ether to give the cis-α,α′-disubstituted piperidine, pyrrolidine and hexahydroazepine, respectively, in high enantiomeric excess.
