84538-49-8

Basic information

• Product Name: 2-(piperidine-1-carbonyl)benzaldehyde
• Synonyms: 2-(piperidine-1-carbonyl)benzaldehyde
• CAS NO: 84538-49-8
• Molecular Weight: 217.268
• Mol File: 84538-49-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-(piperidine-1-carbonyl)benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(piperidine-1-carbonyl)benzaldehyde(84538-49-8)
• EPA Substance Registry System: 2-(piperidine-1-carbonyl)benzaldehyde(84538-49-8)

Safety Data

• Hazardous Substances Data: 84538-49-8(Hazardous Substances Data)

Usage

General Description

2-(piperidine-1-carbonyl)benzaldehyde is a chemical compound with the molecular formula C16H17NO2. It is an aldehyde derivative that contains a piperidine ring and a benzene ring, as well as a carbonyl group attached to the piperidine ring. This chemical is commonly used as a building block in organic synthesis and medicinal chemistry. It can be used as a key intermediate in the synthesis of various pharmaceuticals, such as antihistamines and antidepressants. Additionally, it has been studied for its potential as an anti-inflammatory and anti-cancer agent. Overall, 2-(piperidine-1-carbonyl)benzaldehyde has important applications in the fields of drug discovery and medicinal chemistry.

Upstream product

• 110-89-4 piperidine 
• 6295-21-2 3-chloro-1(3H)-isobenzofuranone 
• 117886-88-1 2-formyl benzoyl chloride 
• 119-67-5 o-carboxybenzaldehyde 
• 33388-67-9 (2-methyl-phenyl)-(piperidin-1-yl)methanone 
• 643-79-8 o-phthalic dicarboxaldehyde 
• 16859-59-9 3-hydroxy-1(3H)-isobenzofuranone 
• 87-41-2 2-benzofuran-1(3H)-one 
• 6940-49-4 3-Bromophthalide 
• 61296-43-3 3-Iodo-1(3H)-isobenzofuranone 

Relevant articles and documents

Photoreactive Composition, Reaction Product, and Method of Producing Reaction Product

A photoreactive composition including a base-reactive compound, a photobase generator that is represented by the following Formula (1) and that generates a base when irradiated with light, and at least one compound selected from the group consisting of a

Gold-catalyzed amide synthesis from aldehydes and amines in aqueous medium

An efficient gold-catalyzed amide synthesis from aldehydes and amines in aqueous medium under mild reaction conditions has been developed.

Effect of Nucleophilicity and Leaving Group Ability on the SN2 Reactions of Amines with (Acyloxy)alkyl α-Halides: A Product Distribution Study

The course of the reaction of amines with (acyloxy)alkyl α-halides has been found to depend on the nucleophilicity of the amines and the leaving group ability of the halides.More nucleophilic amines tended to give acylated products 2 from the reaction while less nucleophilic amines gave alkylated products 3.The use of a better leaving group also tended to favor the formation of a greater amount of alkylated product.These results have been compared to the observations of Westaway on the effect of leaving group ability and nucleophilicity on the bond lengths in the transit ion state of SN2 reactions.In addition, secondary amines have been shown to cause the rearrangement of 2-formylbenzamides to 3-amino-1(3H)-isobenzofuranones.