132462-23-8

Basic information

• Product Name: 1-benzyl-5,5-(ethylenedioxy)-2-piperidinecarbonitrile
• Synonyms: 1-benzyl-5,5-(ethylenedioxy)-2-piperidinecarbonitrile
• CAS NO: 132462-23-8
• Molecular Formula: C₁₅H₁₈N₂O₂
• Molecular Weight: 258.319
• Mol File: 132462-23-8.mol

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1-benzyl-5,5-(ethylenedioxy)-2-piperidinecarbonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 1-benzyl-5,5-(ethylenedioxy)-2-piperidinecarbonitrile(132462-23-8)
• EPA Substance Registry System: 1-benzyl-5,5-(ethylenedioxy)-2-piperidinecarbonitrile(132462-23-8)

Safety Data

• Hazardous Substances Data: 132462-23-8(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
1-benzyl-5,5-(ethylenedioxy)-2-piperidinecarbonitrile is used as a building block in the synthesis of various pharmaceuticals and organic compounds. Its unique structure allows for the creation of a wide range of molecules with potential therapeutic properties.
Used in Organic Synthesis:
In the field of organic synthesis, 1-benzyl-5,5-(ethylenedioxy)-2-piperidinecarbonitrile serves as a key intermediate for the preparation of complex organic molecules. Its versatility in chemical reactions makes it a valuable component in the synthesis of various organic compounds.
Used in Antiviral and Antimicrobial Applications:
1-benzyl-5,5-(ethylenedioxy)-2-piperidinecarbonitrile has been studied for its potential as an antiviral and antimicrobial agent. Its ability to interact with specific biological targets makes it a candidate for the development of new treatments against viral and bacterial infections.
Used in Neurological Disorder Treatment:
1-benzyl-5,5-(ethylenedioxy)-2-piperidinecarbonitrile has also been investigated for its potential role in the treatment of neurological disorders. Its interaction with specific receptors and pathways in the nervous system suggests that it may have therapeutic benefits for conditions such as Alzheimer's disease, Parkinson's disease, and other neurodegenerative disorders.
However, due to the complex structure and potential biological activity of 1-benzyl-5,5-(ethylenedioxy)-2-piperidinecarbonitrile, further research is necessary to fully understand its properties and explore its potential applications in various industries.

Upstream product

• 127364-04-9 1-Benzyl-3,3-(ethylenedioxy)piperidine 
• 50606-58-1 N-benzyl-3-piperidinone hydrochloride 
• 151-50-8 potassium cyanide 
• 132462-22-7 1-Benzyl-5,5-(ethylenedioxy)-2-piperidinone 

Downstream Products

• 134334-33-1 1-Benzyl-5-(ethylenedioxy)-2-piperidinecarboxaldehyde 
• 134334-34-2 1-Benzyl-5-(ethylenedioxy)-2-piperidinemethanamine 
• 132462-36-3 1-Benzyl-5,5-(ethylenedioxy)-2-(2-phenylethyl)piperidine 
• 132462-35-2 7-Benzyl-8-hydroxymethyl-1,4-dioxa-7-aza-spiro[4.5]decane-8-carbonitrile 
• 132462-37-4 1-Benzyl-5,5-(ethylenedioxy)-2-piperidinemethanol 
• 134334-46-6 N-(7-Benzyl-1,4-dioxa-7-aza-spiro[4.5]dec-8-ylmethyl)-2-chloro-N-(2-methoxy-phenyl)-acetamide 
• 134334-45-5 N-(7-Benzyl-1,4-dioxa-7-aza-spiro[4.5]dec-8-ylmethyl)-2-chloro-N-phenyl-acetamide 
• 134334-42-2 1-Benzyl-5-(ethylenedioxy)-N-(2-methoxyphenyl)-2-piperidinemethanamine 
• 134334-44-4 7-(Ethylenedioxy)-2-(2-methoxyphenyl)octahydro-2H-pyrido<1,2-a>pyrazin-3-one 
• 134334-35-3 N-(7-Benzyl-1,4-dioxa-7-aza-spiro[4.5]dec-8-ylmethyl)-2-chloro-acetamide 
• 134334-41-1 1-Benzyl-5-(ethylenedioxy)-N-phenyl-2-piperidine-methanamine 
• 134334-48-8 C₁₇H₂₄N₂O₃ 
• 134334-43-3 7-(Ethylenedioxy)-2-phenyloctahydro-2H-pyrido<1,2-a>-pyrazin-3-one 
• 134334-50-2 Hexahydro-2-(2-methoxyphenyl)-2H-pyrido<1,2-a>pyrazin-7(6H)-one 

Relevant articles and documents

Regioselective Oxidation of Piperidine-3 Derivatives: A Synthetic Route to 2,5-Substituted Piperidines

Mercuric acetate oxidation of 1-benzyl-3,3-(ethylenedioxy)piperidine (1) and of 3-CO2Et- and 3-CH2OH-substituted piperidines 7-9 was shown to occur regioselectively at the 6-position.Trapping of the resulting 6-iminium ions with cyanide yielded the corres