138030-54-3

Basic information

• Product Name: ethyl 1-((pyridin-4-yl)methyl) piperidine-4-carboxylate
• Synonyms: ethyl 1-((pyridin-4-yl)methyl) piperidine-4-carboxylate;1-(4-Pyridinylmethyl)-4-piperidinecarboxylic acid ethyl ester;ethyl 1-((pyridin-4-yl)Methyl;4-Piperidinecarboxylic acid,1-(4-pyridinylmethyl)-,ethyl ester
• CAS NO: 138030-54-3
• Molecular Formula: C14H20N2O2
• Molecular Weight: 248.32
• Product Categories: Pyridines
• Mol File: 138030-54-3.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 348.35 °C at 760 mmHg
• Flash Point: 164.477 °C
• Appearance: /
• Density: 1.112
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.535
• CAS DataBase Reference: ethyl 1-((pyridin-4-yl)methyl) piperidine-4-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 1-((pyridin-4-yl)methyl) piperidine-4-carboxylate(138030-54-3)
• EPA Substance Registry System: ethyl 1-((pyridin-4-yl)methyl) piperidine-4-carboxylate(138030-54-3)

Safety Data

• Hazardous Substances Data: 138030-54-3(Hazardous Substances Data)

Usage

General Description

Ethyl 1-((pyridin-4-yl)methyl) piperidine-4-carboxylate is a chemical compound with the molecular formula C15H22N2O2. It is a derivative of piperidine and contains a pyridine ring. ethyl 1-((pyridin-4-yl)methyl) piperidine-4-carboxylate is commonly used in organic synthesis and medicinal chemistry as a building block for the synthesis of various pharmaceuticals and bioactive molecules. It has been reported to exhibit antinociceptive (pain-relieving) effects in experimental studies, suggesting potential applications in the development of analgesic drugs. Overall, ethyl 1-((pyridin-4-yl)methyl) piperidine-4-carboxylate is a versatile chemical that has important implications in both the pharmaceutical and research industries.

InChI:InChI=1/C14H20N2O2/c1-2-18-14(17)13-5-9-16(10-6-13)11-12-3-7-15-8-4-12/h3-4,7-8,13H,2,5-6,9-11H2,1H3

Upstream product

• 872-85-5 pyridine-4-carbaldehyde 
• 1126-09-6 4-carbethoxypiperidine 

Downstream Products

• 1246290-31-2 C₂₂H₃₄N₄O 
• 1246290-30-1 C₂₂H₂₈N₄O 
• 460092-58-4 C₂₃H₃₀N₄O 
• 1246290-33-4 C₂₄H₃₁N₃O₂ 
• 1246290-34-5 C₂₄H₂₉N₃O₂ 
• 1215120-87-8 C₂₅H₃₁N₅O₂ 

Relevant articles and documents

The synthesis and structure-activity relationship of 4-benzimidazolyl- piperidinylcarbonyl-piperidine analogs as histamine H3 antagonists

A structure-activity relationship study of the lead piperazinylcarbonylpiperidine compound 3 resulted in the identification of 4-benzimidazolyl-piperidinylcarbonyl-piperidine 6h as a histamine-3 (H 3) receptor antagonist. Additional optimizatio

1-(4-PIPERIDINYL) BENZIMIDAZOLONES AS HISTAMINE H3 ANTAGONISTS

Disclosed are histamine H3 antagonists of the formula (I) wherein R1 is benzimidazolone derivative, M1 and M2 are optionally substituted carbon or nitrogen, R2 includes optionally substituted aryl or heteroaryl, and the remaining variables are as defined