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2-Acetylaminomethyl pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58481-18-8

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58481-18-8 Usage

Chemical Structure

Contains a pyridine ring with an acetylaminomethyl group attached

Usage in Pharmaceutical Industry

Acts as an intermediate for synthesizing various pharmaceutical drugs

Potential as a Ligand

Studied for its suitability as a ligand in coordination chemistry

Antimicrobial Properties

Investigated for its antimicrobial effects

Interest in Organic Chemistry

Attracts attention due to its unique chemical structure

Potential Applications

Holds promise for further research and potential applications

Check Digit Verification of cas no

The CAS Registry Mumber 58481-18-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,4,8 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 58481-18:
(7*5)+(6*8)+(5*4)+(4*8)+(3*1)+(2*1)+(1*8)=148
148 % 10 = 8
So 58481-18-8 is a valid CAS Registry Number.

58481-18-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(pyridin-2-ylmethyl)acetamide

1.2 Other means of identification

Product number -
Other names 2-acetylaminomethylpyridine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:58481-18-8 SDS

58481-18-8Relevant academic research and scientific papers

Thionyl chloride-mediated synthesis of 2-azaindolizine sulfur-bridged dimers by C-H bond direct chalcogenation of imidazo[1,5-a]pyridines

Kulkarni, Mahesh R.,Lad, Nitin P.,Patil, Shashikant M.,Gaikwad, Nitin D.

, p. 1887 - 1894 (2020/05/04)

Thionyl chloride-mediated chalcogenation of imidazo[1,5-a]pyridine serves as a new protocol for the synthesis of rare bisimidazopyridyl sulfides. This method provides the new route to synthesis of 2-azaindolizine sulfur-bridged dimers called chalcogenide

New half-sandwich (η6-p-cymene)ruthenium(II) complexes with benzothiazole hydrazone Schiff base ligand: Synthesis, structural characterization and catalysis in transamidation of carboxamide with primary amines

Vijayapritha, Subbarayan,Viswanathamurthi, Periasamy

supporting information, (2020/10/18)

Few half-sandwich (η6-p-cymene) ruthenium(II) complexes supported by benzothiazole hydrazone Schiff bases were synthesized. The new complexes possess the general formulae [Ru(η6-p-cymene)(L)Cl] (1-3) (L = salicyl((2-(benzothiazol-2-yl)hydrazono)methylphenol) (SAL-HBT), 2-((2-(benzothiazol-2-yl)hydrazono)methyl)-6 methoxyphenol) (VAN-HBT) or naphtyl-2-((2-(benzothiazol-2-yl)hydrazono)methyl phenol) (NAP-HBT). All compounds were fully studied by analytical, spectroscopic techniques (IR, NMR) and also by mass spectrometry. The solid state structure of the complex 3 reveals the coordination of p-cymene moieties with ruthenium(II) in a three-legged piano-stool geometry along with benzothiazole hydrazone Schiff base ligand in a monobasic bidentate fashion. The catalytic properties of the complexes were screened in transamidation of primary amide with amines after optimization with respect to solvent, substituents, time and catalyst loading. The results show that the complex 3 is the most efficient catalyst for the transamidation of carboxamides with amines.

Phenysilane and Silicon Tetraacetate: Versatile Promotors for Amide Synthesis

Morisset, Eléonore,Chardon, Aurélien,Rouden, Jacques,Blanchet, Jér?me

supporting information, p. 388 - 392 (2020/01/24)

Phenylsilane was reevaluated as a useful coupling reagent for amide synthesis. At room temperature, a wide range of amides and peptides were obtained in good to excellent yields (up to 99 %). For the first time, Weinreb amides synthesis mediated by a hydrosilane were also documented. Comparative experiments with various acetoxysilanes suggested the involvement of a phenyl-triacyloxysilane. From this mechanistic study, silicon tetraacetate was shown as an efficient amine acylating agent.

Metal-Free C-C Coupling of an Allenyl Sulfone with Picolyl Amides to Access Vinyl Sulfones via Pyridine-Initiated in Situ Generation of Sulfinate Anion

Omer, Humair M.,Liu, Peng,Brummond, Kay M.

, p. 7959 - 7975 (2020/07/15)

Vinyl sulfones are privileged motifs known for their biological activity and synthetic utility. Synthetic transformations to efficiently access high-value compounds with these motifs are desired and sought after. Herein, a new procedure is described to fo

Efficient Preparation of Imidazo[1,5- a ]pyridine-1-carboxylic Acids

Tverdiy, Dmytro O.,Chekanov, Maksym O.,Savitskiy, Pavlo V.,Syniugin, Anatolii R.,Yarmoliuk, Sergiy M.,Fokin, Andrey A.

, p. 4269 - 4277 (2016/11/26)

We report a novel and efficient approach to the synthesis of imidazo[1,5-a]pyridine-1-carboxylic acids. By using the reaction of 2-(aminomethyl)pyridine with acyl chlorides followed by one-pot treatment with trifluoroacetic anhydride, 2,2,2-trifluoro-1-im

Ceric ammonium nitrate-mediated detritylation of tritylated amines

Pattanayak, Sankha,Sinha, Surajit

experimental part, p. 34 - 37 (2011/02/25)

Efficient deprotection of tritylated amines to the corresponding amines mediated by 20 mol % ceric ammonium nitrate [Ce(NH4) 2(NO3)6, CAN], 10 equiv of acetic acid and 15 equiv of water in dichloromethane is presented. This method equally worked well in the case of morpholino nucleosides.

Microwave-assisted preparation of amides using a stable and reusable mesoporous carbonaceous solid acid

Luque, Rafael,Budarin, Vitaly,Clark, James H.,MacQuarrie, Duncan J.

experimental part, p. 459 - 461 (2010/04/22)

An efficient and green microwave assisted protocol to prepare amides from amines via N-acylation using acidic polysaccharide derived mesoporous materials provides quantitative yields of amides in short reaction times.

Inhibitory activity of a ceramide library on interleukin-4 production from activated T cells

Park, Jin,Li, Qian,Chang, Young-Tae,Kim, Tae Sung

, p. 2589 - 2595 (2007/10/03)

Allergic diseases are hypersensitivity disorders associated with the production of specific immunoglobulin E (IgE) to environmental allergens. Interleukin (IL)-4, produced primarily by CD4+ T cells, is an important stimulus for the switch of th

The synthesis and biological characterization of a ceramide library

Chang, Young-Tae,Choi, Jaehwa,Ding, Sheng,Prieschl, Eva E.,Baumruker, Thomas,Lee, Jae-Mok,Chung, Sung-Kee,Schultz, Peter G.

, p. 1856 - 1857 (2007/10/03)

A facile synthesis of a combinatorial ceramide library and their activities in the NF-κB pathway and in apoptosis induction/prevention were demonstrated. A novel NF-κB activating molecule was discovered among ceramide containing β-galactose, and the structural requirements of ceramides for apoptosis induction was elucidated. Copyright

Photocatalyzed [2 + 2 + 2]-cycloaddition of nitriles with acetylene: An effective method for the synthesis of 2-pyridines under mild conditions

Heller, Barbara,Sundermann, Bernd,Buschmann, Helmut,Drexler, Hans-Joachim,You, Jingsong,Holzgrabe, Ulrike,Heller, Eberhard,Oehme, Guenther

, p. 4414 - 4422 (2007/10/03)

The photocatalyzed [2 + 2 + 2]-cycloaddition of nitriles with 2 equiv of acetylene to 2-pyridines can be carried out under mild conditions and represents a valuable extension to common synthetical methods. For the ideal wavelength range (350-500 nm), lamps as well as sunlight can be used. Working at room temperature and in organic solvents such as toluene or hexane as well as in water gives satisfying results in many cases. However, it is also possible to vary the solvent and the reaction temperature of the photocatalyzed synthesis and to choose, with respect to the specific substrate, specific requirements for this particular reaction and general requirements of the method. This simple and selective method derives its potential mainly from the large variety of applicable nitriles. Suitable substrates include (functionalized) aliphatic and aromatic nitriles as well as cyanamides derived from secondary amines.

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