176910-35-3 Usage
Spiro compound
Bicyclic structure with a quaternary carbon atom
The compound has two rings connected by a shared carbon atom, which is bonded to four other carbon atoms.
Synonyms
8-Acetyloxacane
An alternative name for the compound, highlighting its structural features.
Applications
Building block in organic synthesis
The compound is used as a starting material for the synthesis of various organic compounds.
Potential uses
Pharmaceuticals and agrochemicals
The compound has potential applications in the development of drugs and chemicals used in agriculture.
Stability
Relatively stable
The compound is not highly reactive and can be stored and used under normal laboratory conditions.
Physical and chemical properties
Interesting and valuable
The compound has unique properties that make it a useful intermediate in the production of other organic compounds.
Ongoing research
Exploring potential uses in different industries
Scientists are continuously studying the compound to find new applications and improve its synthesis methods.
Check Digit Verification of cas no
The CAS Registry Mumber 176910-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,9,1 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 176910-35:
(8*1)+(7*7)+(6*6)+(5*9)+(4*1)+(3*0)+(2*3)+(1*5)=153
153 % 10 = 3
So 176910-35-3 is a valid CAS Registry Number.
176910-35-3Relevant articles and documents
Eclipsed Conformation of the Exocyclic N-CH2 Bond in N-Neopentylpiperidines and the Stereodynamic Consequences As Studied by Dynamic NMR Spectroscopy and Molecular Mechanics Calculations
Anderson, J. Edgar,Ijeh, Anthony I.,Storch, Christine,Casarini, Daniele,Lunazzi, Lodovico
, p. 3310 - 3317 (1998)
The dynamic stereochemistry of a range of N-neopentylpiperidines 1 with an eclipsed N-CH2-t-Bu bond is compared with that of the corresponding range of N-ethylpiperidines 2 with a gauche N-CH2Me bond. By using dynamic NMR spectroscopy, the relative importance of ring inversion, exocyclic bond rotation, and nitrogen inversion are elucidated and barriers are reported and discussed. Minor populations of the neopentyl-axial-eclipsed conformation are detected directly and identified with the help of molecular mechanics calculations. The corresponding N-alkylpyrrolidines are also reported.
Ring cleavage reaction of heterocyclic ketones based on crossed aldol condensation
Suemune, Hiroshi,Uchida, Jun,Sakai, Kiyoshi
, p. 625 - 631 (2007/10/03)
Ring cleavage reaction based on crossed aldol condensation using heterocyclic ketones such as 4-piperidone and nortropinone derivatives with benzaldehyde under acetalization conditions (BF3-Et2O/ethylene glycol) has been achieved.
