202145-29-7 Usage
General Description
The chemical compound [(4-chlorophenyl)methyl][(4-methoxyphenyl)methyl]amine, also known as N-(4-chlorobenzyl)-N-(4-methoxybenzyl)amine, is a tertiary amine with the molecular formula C15H16ClNO. It is a chiral molecule with two asymmetric carbon atoms, resulting in four possible stereoisomers. [(4-chlorophenyl)methyl][(4-methoxyphenyl)methyl]amine is commonly used as an intermediate or building block in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It can also be utilized in the production of dyes, perfumes, and other fine chemicals. Additionally, it may have potential biological activity and therapeutic applications, although specific uses and properties may vary depending on the particular stereoisomer. Overall, [(4-chlorophenyl)methyl][(4-methoxyphenyl)methyl]amine is an important and versatile chemical with a wide range of applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 202145-29-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,2,1,4 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 202145-29:
(8*2)+(7*0)+(6*2)+(5*1)+(4*4)+(3*5)+(2*2)+(1*9)=77
77 % 10 = 7
So 202145-29-7 is a valid CAS Registry Number.
202145-29-7Relevant articles and documents
Stereocontrolled Synthesis of β-Lactams within [2]Rotaxanes: Showcasing the Chemical Consequences of the Mechanical Bond
Martinez-Cuezva, Alberto,Lopez-Leonardo, Carmen,Bautista, Delia,Alajarin, Mateo,Berna, Jose
, p. 8726 - 8729 (2016)
The intramolecular cyclization of N-benzylfumaramide [2]rotaxanes is described. The mechanical bond of these substrates activates this transformation to proceed in high yields and in a regio- and diastereoselective manner, giving interlocked 3,4-disubstituted trans-azetidin-2-ones. This activation effect markedly differs from the more common shielding protection of threaded functions by the macrocycle, in this case promoting an unusual and disfavored 4-exo-trig ring closure. Kinetic and synthetic studies allowed us to delineate an advantageous approach toward β-lactams based on a two-step, one-pot protocol: an intramolecular ring closure followed by a thermally induced dethreading step. The advantages of carrying out this cyclization in the confined space of a benzylic amide macrocycle are attributed to its anchimeric assistance.
