150717-69-4 Usage
Chemical structure
A derivative of butanone and piperidine with a 4-chlorophenyl group, a 4-hydroxy-1-piperidinyl group, and a 4-nitrophenyl group.
Molecular weight
Approximately 399.86 g/mol
Appearance
Likely a solid or oily liquid, depending on the temperature
Solubility
Soluble in organic solvents such as ethanol, methanol, and acetone
Stability
Stable under normal temperature and pressure conditions, but sensitive to heat, light, and moisture
Reactivity
May react with strong acids, strong bases, and nucleophiles
Pharmaceutical industry
As a building block for the synthesis of various organic compounds
Medicinal chemistry
Due to the presence of piperidine and phenyl groups, it may exhibit various pharmacological activities and properties
Safety precautions
Handle with care, as it may be toxic or harmful if inhaled, ingested, or absorbed through the skin. Use appropriate personal protective equipment (PPE) and follow proper disposal procedures.
Further research and development
Of interest for its potential applications in the field of medicinal chemistry, warranting further investigation into its pharmacological properties and possible therapeutic uses.
Check Digit Verification of cas no
The CAS Registry Mumber 150717-69-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,7,1 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 150717-69:
(8*1)+(7*5)+(6*0)+(5*7)+(4*1)+(3*7)+(2*6)+(1*9)=124
124 % 10 = 4
So 150717-69-4 is a valid CAS Registry Number.
150717-69-4Relevant articles and documents
Microwave-accelerated fluorodenitrations and nitrodehalogenations: expeditious routes to labeled PET ligands and fluoropharmaceuticals
LaBeaume, Paul,Placzek, Michael,Daniels, Mathew,Kendrick, Ian,Ng, Patrick,McNeel, Melissa,Afroze, Roushan,Alexander, Abigail,Thomas, Rhiannon,Kallmerten, Amy E.,Jones, Graham B.
scheme or table, p. 1906 - 1909 (2010/09/07)
Methods for the expeditious fluorination of arenes have been investigated, using readily available fluoride sources. An optimized procedure for microwave-accelerated fluorodenitration has been developed, giving good to excellent yields in less than 10 min, rendering it practical for use in the preparation of F18 labeled ligands for PET imaging. Application of the method in the synthesis of CNS agents is demonstrated, and a practical method for the preparation of substrates is also presented.
