61893-82-1 Usage
Description
N-(3,4-dimethoxybenzyl)pyridin-2-amine is a chemical compound with the molecular formula C15H17N3O2. It is an organic compound containing a pyridine ring, an amine group, and a benzyl group with two methoxy substituents. N-(3,4-dimethoxybenzyl)pyridin-2-amine has potential biological activities and is used in pharmaceutical research and development. Its chemical structure and properties make it a valuable building block for the synthesis of new organic molecules with potential pharmacological activities.
Uses
Used in Pharmaceutical Research and Development:
N-(3,4-dimethoxybenzyl)pyridin-2-amine is used as a chemical intermediate for the synthesis of new organic molecules with potential pharmacological activities. Its unique structure allows for the development of novel compounds that can target specific biological pathways and address various medical conditions.
Used in Drug Discovery:
N-(3,4-dimethoxybenzyl)pyridin-2-amine is used as a potential therapeutic agent for various medical conditions. Its biological activities and chemical properties make it a promising candidate for drug discovery, where it can be further optimized and developed into effective treatments for a range of diseases and disorders.
Used in Organic Synthesis:
N-(3,4-dimethoxybenzyl)pyridin-2-amine is used as a building block in organic synthesis, allowing chemists to create new compounds with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science. Its versatile structure enables the development of innovative molecules with unique properties and functions.
Check Digit Verification of cas no
The CAS Registry Mumber 61893-82-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,8,9 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61893-82:
(7*6)+(6*1)+(5*8)+(4*9)+(3*3)+(2*8)+(1*2)=151
151 % 10 = 1
So 61893-82-1 is a valid CAS Registry Number.
61893-82-1Relevant articles and documents
Ru(II)-NHC catalysed N-Alkylation of amines with alcohols under solvent-free conditions
Karaca, Emine ?zge,Dehimat, Zieneb Imene,Ya?ar, Sedat,Gürbüz, Nevin,Tebbani, Dahmane,?etinkaya, Bekir,?zdemir, ?smail
, (2021/04/02)
The reaction of [RuCl2(p-cymene)]2 with in situ prepared Ag-N-heterocyclic carbene (NHC) complexes yields a series of [RuCl2(p-cymene)(NHC)] complexes (2). All of the complexes have been characterised by elemental analysis, and 1H NMR and 13C NMR spectroscopies. These complexes have been tested for the N-alkylation of aromatic amines with arylmethyl alcohols under neat conditions in the presence of KOtBu at 120 °C. Compounds (2) are stable and have high catalytic/selective activity for the N-alkylation reactions of primary amines to afford secondary amines.
Novel N-Alkylbenzimidazole-Ruthenium (II) complexes: Synthesis and catalytic activity of N-alkylating reaction under solvent-free medium
?ahin, Neslihan,?zdemir, Nam?k,Gürbüz, Nevin,?zdemir, ?smail
, (2019/01/04)
In this article, direct N-alkylation reactions of amines with alcohols derivatives have been investigated. For this purpose, a new series ruthenium (II) complexes bearing N-coordinated benzimidazole complexes with have been synthesized and fully characterized by elemental analysis, FT-IR, 1H NMR and, 13C NMR spectroscopies. Additionally, the structures of the complexes 2b and 2c have been confirmed by X-ray crystallography. Although the N-alkylating reaction is usually performed in toluene, the catalytic study of complexes 2a-d has carried out no additional solvent and alcohol acted both as solvent and reactant of alkylating by using a little excess of alcohols. Surprisingly, conversion and selectivity of amine product for alkylation reaction have been seen high in medium solvent-free relative to in toluene.