1424-65-3 Usage
Uses
Used in Pharmaceutical Synthesis:
4-Dibenzylamino-2-methylbenzo-aldehyde is used as a key intermediate in the synthesis of pharmaceuticals, playing a crucial role in the development of new drugs and medications. Its unique chemical structure allows for the creation of a wide range of therapeutic compounds.
Used in Organic Compounds Synthesis:
4-Dibenzylamino-2-methylbenzo-aldehyde is also utilized in the synthesis of various organic compounds, serving as a building block for the creation of complex molecules with potential applications in different fields.
Used in Fragrance Production:
4-Dibenzylamino-2-methylbenzo-aldehyde is used as a fragrance ingredient, capitalizing on its aromatic properties to create scents for perfumes, cosmetics, and other scented products.
Used in Flavor Production:
Similarly, its aldehydic characteristics make it a valuable component in the production of flavors for food and beverages, enhancing the taste and aroma of various products.
Used in Organic Chemistry Research:
4-Dibenzylamino-2-methylbenzo-aldehyde is used as a reagent in organic chemistry, facilitating various chemical reactions and contributing to the advancement of scientific knowledge in this field.
Used in Medicinal and Therapeutic Applications:
4-Dibenzylamino-2-methylbenzo-aldehyde is being explored for its potential pharmacological properties, with ongoing research aimed at identifying its possible use in medicinal and therapeutic applications, further expanding its utility in the healthcare sector.
Check Digit Verification of cas no
The CAS Registry Mumber 1424-65-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,2 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1424-65:
(6*1)+(5*4)+(4*2)+(3*4)+(2*6)+(1*5)=63
63 % 10 = 3
So 1424-65-3 is a valid CAS Registry Number.
InChI:InChI=1/C22H21NO/c1-18-14-22(13-12-21(18)17-24)23(15-19-8-4-2-5-9-19)16-20-10-6-3-7-11-20/h2-14,17H,15-16H2,1H3
1424-65-3Relevant academic research and scientific papers
Selective Monoamine Oxidase Inhibitors. 4. 4-Aminophenethylamine Derivatives with Neuron-Selective Action
Florvall, Lennart,Fagervall, Ingrid,Ask, Anna-Lena,Ross, Svante B.
, p. 2250 - 2256 (2007/10/02)
Nine 4-aminophenethylamine derivatives were synthesized and tested for monoamine oxidase (MAO) inhibitory effects with particular attention to their selectivity for MAO within monoaminergic neurons in the rat brain.All compounds selectively inhibited the A form of MAO in vitro.Some of the compounds inhibited the MAO within the monoaminergic neurons at much lower doses than those required for inhibition of MAO within other cells in vivo.The most potent compounds in this respect were 4-amino-2-fluoro-α-methylphenethylamine (5) and 4-amino-2-chloro-α-methylphenethylamine (4).
