202145-29-7 Usage
Uses
Used in Pharmaceutical Industry:
[(4-chlorophenyl)methyl][(4-methoxyphenyl)methyl]amine is used as an intermediate or building block for the synthesis of various pharmaceuticals. Its unique structure allows for the creation of complex molecules with specific therapeutic properties, contributing to the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical industry, [(4-chlorophenyl)methyl][(4-methoxyphenyl)methyl]amine is utilized as a component in the production of various agrochemicals. Its versatility in organic synthesis enables the development of compounds with targeted effects on pests or other agricultural concerns.
Used in Dye Production:
[(4-chlorophenyl)methyl][(4-methoxyphenyl)methyl]amine is also used as a building block in the production of dyes. Its chemical properties make it suitable for creating dyes with specific color characteristics and stability, catering to various applications in the textile, printing, and other industries.
Used in Perfumery:
[(4-chlorophenyl)methyl][(4-methoxyphenyl)methyl]amine is employed in the perfume industry as a component in the creation of various fragrances. Its unique chemical structure can contribute to the development of distinct and complex scents.
Used in Fine Chemicals Industry:
Additionally, [(4-chlorophenyl)methyl][(4-methoxyphenyl)methyl]amine is used in the production of other fine chemicals, where its specific properties can be harnessed for specialized applications, such as in the synthesis of advanced materials or chemical intermediates.
Potential Therapeutic Applications:
While not explicitly mentioned in the provided materials, the potential biological activity of [(4-chlorophenyl)methyl][(4-methoxyphenyl)methyl]amine suggests that it may have therapeutic applications. Further research and development could lead to the discovery of new uses in the medical field, depending on the specific stereoisomer and its properties.
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 academic research and scientific papers
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.
Use of polymer supported reagents for clean multi-step organic synthesis: Preparation of amines and amine derivatives from alcohols for use in compound library generation
Ley, Steven V.,Bolli, Martin H.,Hinzen, Berthold,Gervois, Anne-Geraldine,Hall, Beverley J.
, p. 2239 - 2241 (2007/10/03)
The automated sequential application of polymer supported perruthenate (PSP) and polymer supported cyanoborohydride (PSCBH) in an oxidation-reductive amination procedure allowed the efficient transformation of simple alcohols into more complex amines which can be further derivatised by the use of polymer bound amino sulfonylpyridinium chlorides.
