73657-71-3

Basic information

• Product Name: 1-benzyl-3-ethyl-1,2,5,6-tetrahydropyridine-2-carbonitrile
• CAS NO: 73657-71-3
• Molecular Formula: C₁₅H₁₈N₂
• Molecular Weight: 226.3168
• Mol File: 73657-71-3.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 366°C at 760 mmHg
• Flash Point: 155.2°C
• Density: 1.06g/cm³
• Vapor Pressure: 1.51E-05mmHg at 25°C
• Refractive Index: 1.569
• CAS DataBase Reference: 1-benzyl-3-ethyl-1,2,5,6-tetrahydropyridine-2-carbonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 1-benzyl-3-ethyl-1,2,5,6-tetrahydropyridine-2-carbonitrile(73657-71-3)
• EPA Substance Registry System: 1-benzyl-3-ethyl-1,2,5,6-tetrahydropyridine-2-carbonitrile(73657-71-3)

Safety Data

• Hazardous Substances Data: 73657-71-3(Hazardous Substances Data)

Usage

Explanation

This compound is derived from a tetrahydropyridine, which is a type of heterocyclic compound containing a six-membered nitrogen-containing ring with four carbon atoms and one nitrogen atom.
3. Benzyl group attachment

Explanation

A benzyl group (C6H5CH2-) is attached to the nitrogen atom in the tetrahydropyridine ring, which contributes to the compound's structure and properties.
4. Ethyl group attachment

Explanation

An ethyl group (C2H5-) is also attached to the nitrogen atom in the tetrahydropyridine ring, further modifying the compound's structure and properties.
5. Carbonitrile group presence

Explanation

The carbonitrile group (C≡N) is present in the molecule, which is a triple-bonded carbon-nitrogen functional group. This group adds to the chemical properties of the compound.
6. Organic synthesis and pharmaceutical research applications

Explanation

Due to its unique structure and potential biological activity, 1-benzyl-3-ethyl-1,2,5,6-tetrahydropyridine-2-carbonitrile is often used in organic synthesis and pharmaceutical research.
7. Potential drug development

Explanation

The compound may have applications in the development of new drugs, as its structure and properties can be exploited to create novel therapeutic agents.
8. Building block for complex organic molecules

Explanation

1-benzyl-3-ethyl-1,2,5,6-tetrahydropyridine-2-carbonitrile can also serve as a building block for the synthesis of more complex organic molecules, which can be used in various chemical and pharmaceutical applications.

Upstream product

• 60900-18-7 1-benzyl-3-ethyl-1,2,5,6-tetrahydropyridine N-oxide 
• 151-50-8 potassium cyanide 
• 536-78-7 3-ethylpyridine 
• 55077-15-1 1-benzyl-3-ethylpyridinium bromide 
• 60900-14-3 1-benzyl-3-ethyl-1,2,5,6-tetrahydropyridine 
• 147185-15-7 1-benzyl-3-ethyl-5,6-dihydropyridinium trifluoroacetate 
• 7677-24-9 trimethylsilyl cyanide 

Downstream Products

• 73658-10-3 1-benzyl-2-cyano-2-deuterio-3-ethyl-3-piperideine 
• 176039-64-8 N-benzyl-3-ethyl-3-piperidein-2-one 
• 73658-11-4 1-benzyl-2-cyano-2-methyl-3-ethyl-3-piperideine 
• 85617-10-3 2-(1-Benzyl-2-cyano-3-ethyl-piperidin-4-yl)-malonic acid dimethyl ester 

Relevant articles and documents

Single electron transfer regioselective photocatalytic synthesis of 2- cyano-1,2,5,6-tetra-hydropyridines

A mild and regioselective single electron transfer (SET) photocatalytic general synthesis of 2-cyano-1,2,5,6-tetrahydropyridines from 1,2,5,6- tetrahydropyridines is described. Cyanotrimethylsilane is used as cyanating agent in the presence of tetraphenyl