921592-86-1 Usage
Chemical structure
The compound consists of a pyrrolidine ring attached to a pyridine ring with an amino group at the 5th position of the pyridine ring.
Chirality
It is a chiral compound, meaning it has a handedness or asymmetry in its molecular structure.
Enantiomers
Different enantiomers (mirror images) of chiral compounds can have different effects in the body.
Pharmaceutical applications
It has potential pharmaceutical applications due to its structure and interaction with biological systems.
Biological activity
The compound may have biological activity in the body, which can be influenced by its chirality.
Drug development
Understanding and controlling the chirality of 1-(5-amino-2-pyridinyl)-3-(R)-pyrrolidinol is important in drug development and medicinal chemistry.
Stereochemistry
The compound has an (R)-configuration at the 3rd position, which is crucial for its potential biological activity and pharmaceutical applications.
Molecular weight
The molecular weight of the compound is approximately 150.23 g/mol.
Solubility
The compound's solubility in water and other solvents can be influenced by its chirality and the presence of functional groups.
Stability
The stability of the compound under various conditions (e.g., temperature, pH, light exposure) can be affected by its chirality and molecular structure.
Synthesis
The synthesis of 1-(5-amino-2-pyridinyl)-3-(R)-pyrrolidinol may involve multiple steps, including the formation of the pyrrolidine and pyridine rings, and the introduction of the amino group at the 5th position.
Purification
The purification of the compound may require techniques such as chromatography to separate enantiomers and remove impurities.
Characterization
Techniques like nuclear magnetic resonance (NMR), mass spectrometry (MS), and infrared (IR) spectroscopy can be used to confirm the structure and purity of the compound.
Safety and handling
Proper safety measures should be taken when handling 1-(5-amino-2-pyridinyl)-3-(R)-pyrrolidinol, including the use of personal protective equipment (PPE) and following good laboratory practices.
Check Digit Verification of cas no
The CAS Registry Mumber 921592-86-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,1,5,9 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 921592-86:
(8*9)+(7*2)+(6*1)+(5*5)+(4*9)+(3*2)+(2*8)+(1*6)=181
181 % 10 = 1
So 921592-86-1 is a valid CAS Registry Number.
921592-86-1Relevant articles and documents
SUBSTITUTED HETEROAROMATIC PYRAZOLE-CONTAINING CARBOXAMIDE AND UREA DERIVATIVES AS VANILLOID RECEPTOR LIGANDS
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, (2013/03/26)
The invention relates to substituted heteroaromatic pyrazole-containing carboxamide and urea derivatives as vanilloid receptor ligands, to pharmaceutical compositions containing these compounds and also to these compounds for use in the treatment and/or prophylaxis of pain and further diseases and/or disorders.
THERAPEUTIC AGENTS
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Page/Page column 26, (2010/11/25)
Compounds of formula (I), processes for preparing such compounds, their use in the treatment of obesity, psychiatric disorders, cognitive disorders, memory disorders, schizophrenia, epilepsy, and related conditions, and neurological disorders such as dementia, multiple sclerosis, Parkinson's disease, Huntington's chorea and Alzheimer's disease and pain related disorders and to pharmaceutical compositions containing them.
