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2198-53-0

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2198-53-0 Usage

Description

2',6'-DIMETHYLACETANILIDE, also known as 2,6-Dimethylacetanilide, is an organic compound derived from acetanilide through electrophilic substitution reaction. It is characterized by its off-white to yellow crystalline needles or crystalline powder appearance. 2',6'-DIMETHYLACETANILIDE is formed by the iodination of chloroacetanilide in the presence of ferroiodide and copper chloride as catalysts, resulting in 4-iodine-2,6-dimethylacetanilide.

Uses

Used in Pharmaceutical Industry:
2',6'-DIMETHYLACETANILIDE is used as an impurity in the production of Lidocaine (L397800), a commonly used local anesthetic and antiarrhythmic medication. Its presence in the manufacturing process is essential for the synthesis of Lidocaine, which is widely utilized in medical and dental procedures to numb specific areas and prevent pain.
Additionally, 2',6'-DIMETHYLACETANILIDE may have potential applications in other industries, such as chemical research or material science, due to its unique chemical properties.

Synthesis Reference(s)

Journal of the American Chemical Society, 106, p. 5759, 1984 DOI: 10.1021/ja00331a073Chemical and Pharmaceutical Bulletin, 30, p. 4242, 1982 DOI: 10.1248/cpb.30.4242Journal of Heterocyclic Chemistry, 2, p. 181, 1965 DOI: 10.1002/jhet.5570020214

Safety Profile

Moderately toxic by ingestion.When heated to decomposition it emits toxic fumes ofNOx.

Check Digit Verification of cas no

The CAS Registry Mumber 2198-53-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,9 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2198-53:
(6*2)+(5*1)+(4*9)+(3*8)+(2*5)+(1*3)=90
90 % 10 = 0
So 2198-53-0 is a valid CAS Registry Number.

2198-53-0 Well-known Company Product Price

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  • Alfa Aesar

  • (B25687)  2',6'-Dimethylacetanilide, 97%   

  • 2198-53-0

  • 25g

  • 396.0CNY

  • Detail
  • Alfa Aesar

  • (B25687)  2',6'-Dimethylacetanilide, 97%   

  • 2198-53-0

  • 100g

  • 938.0CNY

  • Detail
  • Sigma-Aldrich

  • (PHR1671)  2′,6′-Dimethylacetanilide (Lidocaine RCC)  pharmaceutical secondary standard

  • 2198-53-0

  • PHR1671-100MG

  • 5,749.38CNY

  • Detail

2198-53-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2,6-dimethylphenyl)acetamide

1.2 Other means of identification

Product number -
Other names Acetamide,N-(2,6-dimethylphenyl)

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:2198-53-0 SDS

2198-53-0Relevant articles and documents

Preparation and catalytic evaluation of a palladium catalyst deposited over modified clinoptilolite (Pd&at;MCP) for chemoselective N-formylation and N-acylation of amines

Amirsoleimani, Mina,Khalilzadeh, Mohammad A.,Zareyee, Daryoush

, (2020/08/22)

Novel palladium nanoparticles stabilized by clinoptilolite as a natural inexpensive zeolite prepared and used for N-formylation and N-acylation of amines at room temperature at environmentally benign reaction conditions in good to excellent yields. Pd (II) was immobilized on the surface of clinoptilolite via facile multi-step amine functionalization to obtain a sustainable, recoverable, and highly active nano-catalyst. The structural and morphological characterizations of the catalyst carried out using XRD, FT-IR, BET and TEM techniques. Moreover, the catalyst is easily recovered using simple filtration and reused for 7 consecutive runs without any loss in activity.

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.

The immobilized Cu nanoparticles on magnetic montmorillonite (MMT?Fe3O4?Cu): As an efficient and reusable nanocatalyst for reduction and reductive-acetylation of nitroarenes with NaBH4

Zeynizadeh, Behzad,Rahmani, Soleiman,Tizhoush, Hengameh

, (2019/11/28)

In this study, the immobilization of copper nanoparticles on superparamagnetic montmorillonite, MMT?Fe3O4?Cu, was studied. Magnetically nanoparticles (MNPs) of iron oxide (Fe3O4) were primarily prepared by a chemical co-precipitation method. Next, the prepared Fe3O4 MNPs were intercalated within the interlamellar spaces and external surface of sodium-exchanged montmorillonite. Finally, Cu NPs were immobilized on magnetic montmorillonite by a simply mixing of an aqueous solution of CuCl2·2H2O with MMT?Fe3O4 followed by the reduction with NaBH4. Characterization of MMT?Fe3O4 clay system represented that through the immobilization of Fe3O4 MNPs, disordered-layers structure of MMT was easily reorganized to an ordered-layers arrangement. The synthesized composite systems were characterized using FT-IR, SEM, EDX, XRD, VSM, BET and ICP-OES analyses. SEM analysis exhibited that dispersion of Cu NPs, with the size distribution of 15–25 nm, on the surface of magnetic clay was taken place perfectly. BET surface analysis indicated that after the immobilization of Fe3O4 and Cu species, the surface area and total pore volume of MMT?Fe3O4?Cu system was decreased. Next, the Cu-clay nanocomposite system showed a perfect catalytic activity towards reduction of nitroarenes to anilines as well as reductive-acetylation of nitroarenes to acetanilides using NaBH4 and Ac2O in water as a green and economic solvent. The copper magnetic clay catalyst can be easily separated from the reaction mixture by an external magnetic field and reused for six consecutive cycles without the significant loss of its catalytic activity.

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