5425-51-4 Usage
Chemical class
Phenol ethers
Explanation
Different sources of media describe the Explanation of 5425-51-4 differently. You can refer to the following data:
1. 1-(2-methylphenoxy)-3-(piperidin-1-yl)propan-2-ol belongs to the class of organic compounds known as phenol ethers.
2. It is a derivative of a piperidine and a phenol ether, containing a piperidine ring with a para-substituted phenol ether moiety.
3. The compound is known for its pharmacological and biological activities, which make it a valuable compound for research and development.
4. 1-(2-methylphenoxy)-3-(piperidin-1-yl)propan-2-ol has applications in the pharmaceutical industry, particularly in the development of drugs for various medical conditions.
5. The compound's unique molecular structure and properties make it a valuable compound for research and development in the field of medicinal chemistry.
6. The molecular structure of 1-(2-methylphenoxy)-3-(piperidin-1-yl)propan-2-ol includes a piperidine ring and a para-substituted phenol ether moiety, which contribute to its pharmacological and biological activities.
7. As an organic compound, 1-(2-methylphenoxy)-3-(piperidin-1-yl)propan-2-ol is likely to be soluble in organic solvents such as ethanol, methanol, or dimethyl sulfoxide (DMSO).
8. The compound is expected to be stable under normal conditions, such as room temperature and pressure, and in the absence of strong acids, bases, or oxidizing agents.
9. 1-(2-methylphenoxy)-3-(piperidin-1-yl)propan-2-ol can be synthesized with high purity, which is essential for its use in pharmaceutical research and development.
10. As with any chemical compound, 1-(2-methylphenoxy)-3-(piperidin-1-yl)propan-2-ol should be handled with care, following proper safety protocols and guidelines to minimize potential hazards.
Derivative
Piperidine and phenol ether
Pharmacological and biological activities
Known for its pharmacological and biological activities
Applications
Pharmaceutical industry
Molecular structure
Unique molecular structure
Functional groups
Contains a piperidine ring and a para-substituted phenol ether moiety
Solubility
Soluble in organic solvents
Stability
Stable under normal conditions
Purity
Synthesized with high purity
Safety
Handle with care
Check Digit Verification of cas no
The CAS Registry Mumber 5425-51-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,2 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5425-51:
(6*5)+(5*4)+(4*2)+(3*5)+(2*5)+(1*1)=84
84 % 10 = 4
So 5425-51-4 is a valid CAS Registry Number.
