57678-45-2 Usage
Uses
Used in Organic Synthesis:
N-[2-(AMINOMETHYL)PHENYL]-N,N-DIMETHYLAMINE is used as a building block for the synthesis of various organic compounds. Its unique structure allows it to participate in a range of chemical reactions, facilitating the creation of new molecules with diverse applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, N-[2-(AMINOMETHYL)PHENYL]-N,N-DIMETHYLAMINE serves as a key intermediate in the development of new drugs. Its ability to form stable complexes with other molecules makes it a valuable component in medicinal chemistry, contributing to the discovery of potential therapeutic agents.
Used in Dye and Pigment Production:
N-[2-(AMINOMETHYL)PHENYL]-N,N-DIMETHYLAMINE is used as a reagent in the production of dyes and pigments. Its chemical properties enable it to contribute to the color and stability of these products, making it an essential component in the formulation of various colorants used across different industries.
Used in Specialty Chemicals:
N-[2-(AMINOMETHYL)PHENYL]-N,N-DIMETHYLAMINE also finds application in the production of specialty chemicals, where its unique properties are harnessed to create high-value products with specific functions. Its versatility in chemical reactions makes it a sought-after ingredient in the development of niche chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 57678-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,6,7 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 57678-45:
(7*5)+(6*7)+(5*6)+(4*7)+(3*8)+(2*4)+(1*5)=172
172 % 10 = 2
So 57678-45-2 is a valid CAS Registry Number.
57678-45-2Relevant academic research and scientific papers
SMALL MOLECULE ACTIVATORS OF NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE (NAMPT) AND USES THEREOF
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Paragraph 00468, (2018/08/03)
Provided herein are small molecule activators of Nicotinamide Phosphoribosyltransferase (NAMPT), compositions comprising the compounds, and methods of using the compounds and compositions.
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.
