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53214-35-0

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53214-35-0 Usage

Description

1-(1H-benzimidazol-2-ylmethyl)pyridinium is a chemical compound characterized by the presence of a benzimidazole ring and a pyridinium group. It is known for its potential pharmaceutical applications and its ability to bind to biological targets, making it a versatile compound in the field of chemistry.

Uses

Used in Coordination Chemistry:
1-(1H-benzimidazol-2-ylmethyl)pyridinium is used as a ligand in coordination chemistry for the formation of metal complexes. Its unique structure allows for the creation of stable complexes with various metal ions, which can be utilized in a range of applications, including catalysis and sensing.
Used in Organic Synthesis:
As an intermediate in organic synthesis, 1-(1H-benzimidazol-2-ylmethyl)pyridinium is employed in the synthesis of complex organic molecules and materials. Its structural features facilitate the formation of diverse chemical products, contributing to the development of new compounds with potential applications in various industries.
Used in Pharmaceutical Applications:
1-(1H-benzimidazol-2-ylmethyl)pyridinium has been studied for its potential pharmaceutical applications due to its ability to bind to biological targets. This property makes it a promising candidate for the development of new drugs targeting specific biological receptors or enzymes, which could be beneficial in the treatment of various diseases and conditions.
Used in the Synthesis of Materials:
1-(1H-benzimidazol-2-ylmethyl)pyridinium's chemical and physical properties also make it useful in the synthesis of complex materials with specific properties. These materials could be applied in various fields, such as electronics, optics, or even in the development of new materials for energy storage or conversion.

Check Digit Verification of cas no

The CAS Registry Mumber 53214-35-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,2,1 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 53214-35:
(7*5)+(6*3)+(5*2)+(4*1)+(3*4)+(2*3)+(1*5)=90
90 % 10 = 0
So 53214-35-0 is a valid CAS Registry Number.

53214-35-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(pyridin-1-ium-1-ylmethyl)-1H-benzimidazole,chloride

1.2 Other means of identification

Product number -
Other names 1-(1H-benzimidazol-2-ylmethyl)-pyridinium,chloride

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:53214-35-0 SDS

53214-35-0Downstream Products

53214-35-0Relevant articles and documents

1-(2′-Benzimidazolylmethyl)-pyridinium ylide in the one-pot synthesis of indolizine and benzimidazo [1,2-a]pyridine derivatives

Belguedj, Roumaissa,Bouacida, Sofiane,Merazig, Hocine,Belfaitah, Ali,Bouraiou, Abdelmalek

, p. 555 - 561 (2015)

Four indolizine derivatives were obtained via 1,3-dipolar cycloaddition reaction of 1-(2′-benzimidazolyl-methyl)pyridinium ylide with various electron-deficient alkynes. The reaction of this pyridinium N-ylide with dimethyl maleate gave an unexpected methyl 1-oxo-benzimidazo [1,2-a]pyridine-3-carboxylate. The structures of all reported compounds have been examined by X-ray crystallography and NMR spectroscopy.

Heterocyclic Betaines. 13. Synthesis and Electronic and Molecular Structures of Methylenepyridinium and Methyleneimidazolium Azolate Inner Salts

Alcalde, Ermitas,Perez-Garcia, Lluisa,Miravitlles, Carlos,Rius, Jordi,Valenti, Eduard

, p. 4829 - 4834 (2007/10/02)

A convenient synthesis of several examples of betaines 3 and 4 is reported.The electronic and molecular structure of the title betaines 3 and 4 is investigated in terms of a single-crystal diffraction X-ray analysis of compound 7, spectroscopic methods, and experimental dipole moment values (12.34-15.34 D).Semiempirical molecular orbital calculations (MNDO and AM1 methods) provide a useful complementary information to the experimental results.

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