72752-53-5 Usage
General Description
(2-Pyrrolidin-1-ylphenyl)methylamine, also known as 2-PMPA, is a chemical compound that belongs to the class of phenylmethylamines. It is a psychoactive compound and acts as a stimulant, which means it can increase alertness, attention, and energy. It is also known to have potential effects on mood and cognitive function. The compound is similar in structure to amphetamine and has been used as a recreational drug. However, it is important to note that the use and possession of (2-Pyrrolidin-1-ylphenyl)methylamine may be illegal in some jurisdictions and can pose serious health risks, including addiction, psychosis, and cardiovascular effects. Therefore, caution should be exercised when dealing with this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 72752-53-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,7,5 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 72752-53:
(7*7)+(6*2)+(5*7)+(4*5)+(3*2)+(2*5)+(1*3)=135
135 % 10 = 5
So 72752-53-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H16N2/c12-9-10-5-1-2-6-11(10)13-7-3-4-8-13/h1-2,5-6H,3-4,7-9,12H2
72752-53-5Relevant articles and documents
Aminoborohydrides. 12. Novel tandem SNAr amination-reduction reactions of 2-halobenzonitriles with lithium N,N-dialkylaminoborohydrides
Thomas,Collins,Cuzens,Spiciarich,Goralski,Singaram
, p. 1999 - 2004 (2007/10/03)
A novel tandem amination-reduction reaction has been developed in which 2-(N,N-dialkylamino)benzylamines are generated from 2-halobenzonitriles and lithium N,N-dialkylaminoborohydride (LAB) reagents. These reactions are believed to occur through a tandem SNAr amination-reduction mechanism wherein the LAB reagent promotes halide displacement by the N,N-dialkylamino group, and the nitrile is subsequently reduced. This one-pot procedure is complimentary to existing synthetic methods and is an attractive synthetic tool for the nucleophilic aromatic substitution of halobenzenes with less nucleophilic amines. The (N,N-dialkylamino)benzylamine products of this reaction are easily isolated after a simple aqueous workup procedure in very good to excellent yields.