175441-83-5 Usage
Description
N-(Diphenylmethylene)-N-[(5-Methylpyridin-3-yl)Methyl]Amine, with the CAS number 175441-83-5, is a chemical compound that is characterized as a yellow oil. It is primarily utilized in the field of organic synthesis, playing a crucial role in the creation of various organic compounds.
Uses
Used in Organic Synthesis:
N-(Diphenylmethylene)-N-[(5-Methylpyridin-3-yl)Methyl]Amine is used as a synthetic building block for the development of a wide range of organic compounds. Its unique chemical structure allows it to participate in various chemical reactions, facilitating the formation of complex molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N-(Diphenylmethylene)-N-[(5-Methylpyridin-3-yl)Methyl]Amine is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its ability to form a diverse array of organic molecules makes it a valuable asset in the development of new drugs with potential therapeutic benefits.
Used in Chemical Research:
N-(Diphenylmethylene)-N-[(5-Methylpyridin-3-yl)Methyl]Amine is also employed in chemical research as a tool to study the properties and reactivity of different organic molecules. Its use in research helps scientists gain a deeper understanding of chemical reactions and mechanisms, ultimately contributing to the advancement of the field.
Used in Material Science:
In the field of material science, N-(Diphenylmethylene)-N-[(5-Methylpyridin-3-yl)Methyl]Amine is used as a component in the development of novel materials with specific properties. Its incorporation into these materials can lead to improved performance characteristics, such as enhanced stability, reactivity, or selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 175441-83-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,4,4 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 175441-83:
(8*1)+(7*7)+(6*5)+(5*4)+(4*4)+(3*1)+(2*8)+(1*3)=145
145 % 10 = 5
So 175441-83-5 is a valid CAS Registry Number.
175441-83-5Relevant articles and documents
Visible-Light-Mediated Umpolung Reactivity of Imines: Ketimine Reductions with Cy2NMe and Water
Wang, Rui,Ma, Mengyue,Gong, Xu,Panetti, Grace B.,Fan, Xinyuan,Walsh, Patrick J.
supporting information, p. 2433 - 2436 (2018/04/27)
A novel carbanionic reactivity of imines mediated by photoredox catalysis is demonstrated. The umpolung imine reactivity is exemplified by proton abstraction from water as a key step in the reduction of benzophenone ketimines to amines (up to 98% yield). Deuterium is introduced into amines efficiently using D2O as an inexpensive deuterium source (≥95% D ratio). The mechanism of this unusual transformation is probed.
ALKALOID COMPOUNDS FOR TREATING DEPRESSION, SUBSTANCE ADDICTIONS, AND INDICATIONS ASSOCIATED WITH CHRONIC INFLAMMATION
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Paragraph 43, (2016/06/21)
Alkaloid compounds described herein are useful for treating disorders associated with monoamine oxidase (MAO) activity, such as depression, pain, smoking cessation, and substance addictions, and/or for treating disorders associated with chronic or low-level inflammation. In some examples, compounds are effective for treating cancers, autoimmune disorders, and other disorders associated with inducible nitric oxide synthase (iNOS).
METHODS OF SYNTHESIZING ANATABINE
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Page/Page column 4, (2011/10/12)
Anatabine is obtained by reacting benzophenoneimine with 3-aminomethyl pyridine to form benzylhydrylidene-pyridin-3-yl-methyl-amine. The benzylhydrylidene-pyridin-3-yl-methyl-amine is treated with a non-nucleophilic base and a dielectrophile, such as cis-1,4-dichloro-2-butene, followed by acidification, then basification, to provide anatabine. The resulting anatabine is substantially free from contaminants and displays good stability. In an alternative embodiment, the benzylhydrylidene-pyridin-3-yl-methyl-amine may be used in the synthesis of other alkaloids such as anabasine, nornicotine, N-methylanabasine, and anabaseine.
