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1-Benzzyl-3-(methoxycarbonyl)pyridinium is a chemical compound with the molecular formula C13H14NO2. It is a derivative of pyridinium, featuring a benzyl group attached to the 1-position and a methoxycarbonyl group at the 3-position. This organic compound is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in organic chemistry. The compound exhibits a cationic nature due to the presence of the pyridinium ring, which can engage in various chemical reactions, such as nucleophilic substitutions and additions. Its structure and reactivity make it a valuable building block in the development of new molecules with specific properties and functions.

7146-29-4

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7146-29-4 Usage

Pyridinium salt

A type of organic compound that contains a positively charged nitrogen atom, which is characteristic of 1-benzyl-3-(methoxycarbonyl)pyridinium.

Benzyl group

A phenyl group (a ring of 6 carbon atoms with alternating single and double bonds) attached to a methyl group (a single carbon atom with three hydrogen atoms), which is attached to the nitrogen atom in 1-benzyl-3-(methoxycarbonyl)pyridinium.

Methoxycarbonyl group

A functional group consisting of a methoxy group (an oxygen atom bonded to a methyl group) and a carbonyl group (a carbon atom double-bonded to an oxygen atom), which is attached to the nitrogen atom in 1-benzyl-3-(methoxycarbonyl)pyridinium.

Intermediate in organic synthesis

1-benzyl-3-(methoxycarbonyl)pyridinium is commonly used as a starting material or intermediate in the synthesis of more complex organic compounds.

Pharmaceutical applications

The compound has potential uses in the development of new drugs and medical treatments due to its unique chemical structure and properties.

Antimicrobial and antifungal properties

1-benzyl-3-(methoxycarbonyl)pyridinium has been studied for its ability to inhibit the growth of microorganisms, such as bacteria and fungi, which could lead to potential applications in treating infections.

Reactant in chemical reactions

The compound serves as a reactant in various chemical reactions, allowing for the formation of new compounds and the exploration of novel chemical processes.

Potential applications

Due to its unique structure and properties, 1-benzyl-3-(methoxycarbonyl)pyridinium has a wide range of potential applications in the fields of chemistry and pharmaceuticals, including the development of new drugs, treatments, and chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 7146-29-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7146-29:
(6*7)+(5*1)+(4*4)+(3*6)+(2*2)+(1*9)=94
94 % 10 = 4
So 7146-29-4 is a valid CAS Registry Number.

7146-29-4Relevant academic research and scientific papers

Pyrrolidines bearing a quaternary α-stereogenic center. Part 2: Access to proline chimeras, stereoselective approach and mechanistic aspects

Trancard, Delphine,Tout, Jean-Baptiste,Giard, Thierry,Chichaoui, Ilhame,Cahard, Dominique,Plaquevent, Jean-Christophe

, p. 3843 - 3847 (2007/10/03)

The present work describes the access to various proline chimeras bearing a quaternary α-stereogenic center, via the Duhamel ring contraction of heterocyclic enamines. Attempts to induce diastereoselectivity are reported. The 'chiral enamine' strategy aff

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