32470-52-3

Basic information

• Product Name: 1-(PIPERIDIN-4-YLMETHYL)PIPERIDINE
• Synonyms: 1-(PIPERIDIN-4-YLMETHYL)PIPERIDINE;4-PIPERIDIN-1-YLMETHYL-PIPERIDINE;1,4'-Methylenedipiperidine;1-(piperidin-4-ylmethyl)piperidine(SALTDATA: 2HCl H2O);1-(4-PiperidinylMethyl)piperidine;1-(4-PIPERIDINYLMETHYL)PIPERIDINE 2HCL HYDRATE
• CAS NO: 32470-52-3
• Molecular Formula: C₁₁H₂₂N₂
• Molecular Weight: 182.31
• Mol File: 32470-52-3.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 260.033°C at 760 mmHg
• Flash Point: 96.09°C
• Appearance: /
• Density: 0.942g/cm³
• Vapor Pressure: 0.013mmHg at 25°C
• Refractive Index: 1.487
• CAS DataBase Reference: 1-(PIPERIDIN-4-YLMETHYL)PIPERIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(PIPERIDIN-4-YLMETHYL)PIPERIDINE(32470-52-3)
• EPA Substance Registry System: 1-(PIPERIDIN-4-YLMETHYL)PIPERIDINE(32470-52-3)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 32470-52-3(Hazardous Substances Data)

Usage

General Description

1-(piperidin-4-ylmethyl)piperidine is a chemical compound that consists of two piperidine rings connected by a piperidin-4-ylmethyl group. It is used as a building block in the synthesis of various pharmaceuticals and organic compounds. The compound has potential applications in drug development and medicinal chemistry due to its unique structure and reactivity. Additionally, it may be utilized as a reagent in chemical reactions and as a starting material for the preparation of complex organic molecules. However, as with any chemical compound, proper handling and safety precautions should be taken when working with 1-(piperidin-4-ylmethyl)piperidine to ensure the safety of the user and the environment.

InChI:InChI=1/C11H22N2/c1-2-8-13(9-3-1)10-11-4-6-12-7-5-11/h11-12H,1-10H2

Upstream product

• 63214-58-4 piperidin-4-yl-piperidin-1-yl-methanone 
• 110-89-4 piperidine 
• 893086-61-8 4-piperidin-1-ylmethyl-piperidine-1-carboxylic acid (4-bromo-phenyl)amide 
• 757949-38-5 4-(piperidine-1-carbonyl)-piperidine-1-carboxylic acid tert-butyl ester 
• 84358-13-4 N-[(tert-butoxy)carbonyl]piperidine-4-carboxylic acid 
• 1192124-16-5 benzyl 4-(piperidin-1-ylmethyl)piperidine-1-carboxylate 
• 34490-39-6 4-((piperidin-1-yl)methyl)pyridine 
• 137076-22-3 tert butyl 4-formylpiperidine-1-carboxylate 
• 123855-51-6 tert-butyl 4-(hydroxymethyl)piperidin-1-carboxylate 
• 6457-49-4 4-piperidinemethanol 
• 184968-88-5 1,1-dimethylethyl 4-(1-piperidinylmethyl)-1-piperidinecarboxylate 

Downstream Products

• 1401619-11-1 (1-(4-chlorobenzyl)-1H-indol-2-yl)(4-(piperidin-1-ylmethyl)piperidin-1-yl)methanone 
• 1401618-65-2 (1-(4-fluorobenzyl)-1H-indol-2-yl)(4-(piperidin-1-ylmethyl)piperidin-1-yl)methanone 
• 893086-61-8 4-piperidin-1-ylmethyl-piperidine-1-carboxylic acid (4-bromo-phenyl)amide 
• 486436-41-3 1-methyl-2-[4-(piperidin-1-yl)methyl-piperidinocarbonyl]-4-(4'-trifluoromethylbiphenyl-2-carbonylamino)-pyrrole 
• 81310-65-8 1-[(E)-2-(3-Bromo-phenyl)-propenyl]-4-piperidin-1-ylmethyl-piperidine 

Relevant articles and documents

Design, synthesis and antitubercular evaluation of benzothiazinones containing a piperidine moiety

We herein report the design and synthesis of benzothiazinones containing a piperidine moiety as new antitubercular agents based on the structure feature of IMB-ZR-1 discovered in our lab. Some of them were found to have good in vitro activity (MIC 1 μg/

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MODULATORS OF ALPHA7 NICOTINIC ACETYLCHOLINE RECEPTORS AND THERAPEUTIC USES THEREOF

Compounds with α7 nicotinic acetylcholine receptor (α7 nAChR) agonistic activity, processes for their preparation, pharmaceutical compositions containing the same and the use thereof for the treatment of neurological and psychiatric diseases.