157846-76-9 Usage
Chemical structure
Pyrrolidine derivative with a phenyl group and a methoxy group attached to a phenoxy group, which is in turn attached to a phenylpropyl group.
Functional groups
Pyrrolidine ring, phenyl group, methoxy group, phenoxy group, and phenylpropyl group.
Applications
Research and pharmaceutical applications, particularly in the study of organic synthesis and medicinal chemistry.
Potential uses
Development of new drugs due to its structural features and potential pharmacological properties.
Chemical properties
The compound may exhibit properties such as solubility in organic solvents, reactivity with various reagents, and the ability to form salts or complexes with other molecules.
Physical properties
The compound may have specific characteristics such as melting point, boiling point, density, and appearance (e.g., color and state at room temperature).
Safety and handling
As with any chemical compound, appropriate safety measures should be taken when handling 1-[3-(2-methoxyphenoxy)-3-phenylpropyl]pyrrolidine, including the use of personal protective equipment and following proper disposal procedures.
Check Digit Verification of cas no
The CAS Registry Mumber 157846-76-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,8,4 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 157846-76:
(8*1)+(7*5)+(6*7)+(5*8)+(4*4)+(3*6)+(2*7)+(1*6)=179
179 % 10 = 9
So 157846-76-9 is a valid CAS Registry Number.
157846-76-9Relevant articles and documents
Synthesis of 3-aryloxy-3-phenylpropanamines as possible antidepressants
Sharma. V. L.,Bhandari, Kalpana,Chatterjee, S. K.,Satyanarayana, K. V.,Dua, P. R.
, p. 393 - 396 (2007/10/02)
Thirteen new 3-aryloxy-3-phenylpropanamines (11-23) have been prepared and their structures elucidated by mass, IR and 1H-NMR spectra and by elemental analysis.Being structurally similar to fluoxetine these compounds have been tested for their effect on g