291544-82-6 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
It belongs to a class of organic compounds containing a piperidine ring with an alcohol group attached to it.
Explanation
The phenyl ring is a six-membered carbon ring with alternating single and double bonds, and the hydroxymethyl group is attached to the 2nd carbon of the ring.
Explanation
It is used as a building block or precursor in the production of various pharmaceuticals and organic compounds due to its unique chemical structure.
Explanation
Studies have shown that 1-[2-(Hydroxymethyl)phenyl]-4-piperidinol may have the ability to reduce the activity of the central nervous system and provide pain relief.
Explanation
Due to its unique chemical structure and properties, it may have other potential applications in the development of new drugs and therapies.
Explanation
The solubility of a compound refers to its ability to dissolve in a solvent, such as water or organic solvents. This information is not provided in the material.
Explanation
The stability of a compound refers to its ability to resist degradation or change under various conditions, such as temperature, light, or exposure to air. This information is not provided in the material.
Explanation
The reactivity of a compound refers to its tendency to undergo chemical reactions with other substances. This information is not provided in the material.
Chemical class
Piperidinol derivative
Structure
Contains a phenyl ring with a hydroxymethyl group attached to the 2nd position
Application
Intermediate in the synthesis of pharmaceuticals and other organic compounds
Pharmacological properties
Potential use as a central nervous system depressant and analgesic
Potential applications
Medicinal chemistry and drug development
Solubility
Not specified in the material provided
Stability
Not specified in the material provided
Reactivity
Not specified in the material provided
Check Digit Verification of cas no
The CAS Registry Mumber 291544-82-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,1,5,4 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 291544-82:
(8*2)+(7*9)+(6*1)+(5*5)+(4*4)+(3*4)+(2*8)+(1*2)=156
156 % 10 = 6
So 291544-82-6 is a valid CAS Registry Number.
291544-82-6Relevant articles and documents
Preparation and Atropisomerism of 1-(2-Aryl)-piperidin-2-ones
Moehrle,Jeandree,Breitmaier,Rohonczy
, p. 473 - 485 (2007/10/03)
Course and rate of the dehydrogenation of N-tertiary piperidines dependent on their substitution in 4-position and on the hydroxy bearing neighbor group were examined, using mercury(II)-EDTA and the model amino alcohols 1a-1e, 3a-3f, 8a-8f and 10a-10f. The results showed that increasing size of 4-substituents and neighbor groups too decreased the rate of reaction. The products from the 2-substituted benzylic alcohols, the 2-piperidones 7a-7g, 9a-9g and 11a-11g demonstrated atropisomerism. In the case of chiral neighbor groups diastereomeric mixtures were formed.
