5073-63-2 Usage
Chemical class
Phenylpiperidines
This compound belongs to a class of organic compounds that have a phenyl group attached to a piperidine ring.
Molecular weight
347.281 g/mol
The molecular weight is the mass of one mole of the compound, which is useful for determining the amount of substance in a given mass.
Synthetic molecule
Not found naturally
This compound is not found in nature and is typically produced in laboratories for research purposes.
Research interest
Pharmacological properties
The compound has been studied for its potential pharmacological properties, making it a subject of interest in the field of medicinal chemistry.
Potential drug candidate
Further development
Due to its structure and properties, the compound is considered a promising target for further study in drug discovery and development.
Structure
1,2,4,5-tetrahydropyrrolo[2,3-c]pyrazole fused with a 2,5-dichlorophenyl and a piperidin-1-ylmethyl group
The compound's structure consists of a tetrahydropyrrolo[2,3-c]pyrazole ring fused with a 2,5-dichlorophenyl group and a piperidin-1-ylmethyl group, which contributes to its unique properties and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 5073-63-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,7 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5073-63:
(6*5)+(5*0)+(4*7)+(3*3)+(2*6)+(1*3)=82
82 % 10 = 2
So 5073-63-2 is a valid CAS Registry Number.
5073-63-2Relevant articles and documents
Chloropolyfluoro-derivatives of ethyl methyl ether
Coe, Paul L.,Rowbotham, Roger A.,Tatlow, John Colin
, p. 9 - 12 (2007/10/03)
Fluorination of 2-chloroethyl methyl ether by potassium tetrafluorocobaltate at 180-250 °C gave various tri-, tetra-, penta-and hexafluoro(2-chloroethyl methyl) ethers. Cobalt trifluoride afforded the same products in poorer recoveries. Structures were established spectroscopically. Cl2-UV and CHClFCHFOCHF2 gave halogeno-ethers by exchange of Cl for both H and also F.
