72752-55-7 Usage
Uses
Used in Pharmaceutical Research:
2-AZEPAN-1-YL-BENZYLAMINE is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs and biologically active compounds. Its unique structure allows for the creation of molecules with diverse therapeutic effects.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-AZEPAN-1-YL-BENZYLAMINE is utilized as a building block for designing molecules with specific pharmacological properties. Its structural versatility aids in the development of compounds that can target various biological pathways and diseases.
Used in Organic Synthesis:
2-AZEPAN-1-YL-BENZYLAMINE is used as a reagent in organic synthesis for its capacity to form new organic materials and compounds with specialized properties. Its presence in reactions can lead to the creation of complex organic structures with potential applications in various industries.
Used in the Production of Organic Materials:
2-AZEPAN-1-YL-BENZYLAMINE is also used as a component in the production of various organic materials, where its unique chemical properties can enhance the characteristics of the final products, such as stability, reactivity, or selectivity in certain applications.
Check Digit Verification of cas no
The CAS Registry Mumber 72752-55-7 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 72752-55:
(7*7)+(6*2)+(5*7)+(4*5)+(3*2)+(2*5)+(1*5)=137
137 % 10 = 7
So 72752-55-7 is a valid CAS Registry Number.
72752-55-7Relevant academic research and scientific papers
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.
