1084-62-4

Basic information

• Product Name: 1-(2-Hydroxyphenyl)-3-(piperidino)-2-propene-1-one
• Synonyms: 1-(2-Hydroxyphenyl)-3-(piperidino)-2-propene-1-one;1-(2-Hydroxyphenyl)-3-piperidino-2-propen-1-one;2'-Hydroxy-β-piperidinoacrylophenone;(E)-1-(2-hydroxyphenyl)-3-(piperidin-1-yl)prop-2-en-1-one
• CAS NO: 1084-62-4
• Molecular Formula: C₁₄H₁₇NO₂
• Molecular Weight: 0
• Mol File: 1084-62-4.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(2-Hydroxyphenyl)-3-(piperidino)-2-propene-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-Hydroxyphenyl)-3-(piperidino)-2-propene-1-one(1084-62-4)
• EPA Substance Registry System: 1-(2-Hydroxyphenyl)-3-(piperidino)-2-propene-1-one(1084-62-4)

Safety Data

• Hazardous Substances Data: 1084-62-4(Hazardous Substances Data)

Usage

General Description

1-(2-Hydroxyphenyl)-3-(piperidino)-2-propene-1-one, also known as piperonyl ketone, is a chemical compound with the molecular formula C13H15NO2. It is an organic compound that belongs to the class of ketones and contains a benzene ring, a piperidine ring, and a propene moiety. It is commonly used as a fragrance ingredient in the manufacturing of perfumes, soaps, and other personal care products. Additionally, piperonyl ketone is also used as a precursor in the synthesis of various pharmaceuticals and agrochemicals. It possesses potential biological activity and has shown to exhibit insecticidal and acaricidal properties, making it useful in the formulation of insecticides and pest control products. However, it is important to handle and use this chemical with caution due to its potential health hazards and toxicity.

Upstream product

• 110-89-4 piperidine 
• 491-38-3 1-benzopyran-4(4H)-one 
• 118-93-4 o-hydroxyacetophenone 
• 106129-86-6 1-(2-hydroxyphenyl)-3-dimethylaminoprop-2-enone 
• 122775-34-2 3-iodo-chromen-4-one 
• 49619-82-1 3-bromo-4H-chromen-4-one 
• 17422-74-1 3-Formylchromone 

Downstream Products

• 59507-94-7 3-amino-4H-chromen-4-one 

Relevant articles and documents

Synthesis of 1-(2-hydroxy-phenyl)-3-piperidin-1-yl-propenone by ultrasonic irradiation

Different 1-(2-hydroxy-phenyl)-3-piperidin-1-yl-propenones have been synthesized by ultrasonic activation from differently substituted 3-formyl chromones and piperidine. Copyright Taylor & Francis Group, LLC.

Reaction of 3-iodochromone with nucleophiles 3. Formation of 2-aminomethylene-3(2h)-benzofuranones by the reaction with secondary amines

3-Iodochromone (4a) easily reacted with secondary amines in the presence of potassium carbonate to give 2-aminomethylene-3(2H)-benzofuranones in good yields. Under similar conditions without potassium carbonate, 4a was reacted with piperidine to give the