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1084-62-4

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1084-62-4 Usage

Description

1-(2-Hydroxyphenyl)-3-(piperidino)-2-propene-1-one, commonly known as piperonyl ketone, is an organic compound with the molecular formula C13H15NO2. It is a member of the ketone class and features a benzene ring, a piperidine ring, and a propene group. Piperonyl ketone is recognized for its potential biological activity and is utilized in various industries due to its diverse applications.

Uses

Used in Fragrance Industry:
1-(2-Hydroxyphenyl)-3-(piperidino)-2-propene-1-one is used as a fragrance ingredient for its aromatic properties in the manufacturing of perfumes, soaps, and other personal care products. Its unique scent contributes to the overall appeal of these products, enhancing their marketability and consumer experience.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 1-(2-Hydroxyphenyl)-3-(piperidino)-2-propene-1-one is used as a precursor in the synthesis of various pharmaceuticals. Its chemical structure allows for the development of new drugs with potential therapeutic benefits.
Used in Agrochemicals:
1-(2-Hydroxyphenyl)-3-(piperidino)-2-propene-1-one also serves as a precursor in the synthesis of agrochemicals, specifically in the development of insecticides and pest control products. Its insecticidal and acaricidal properties make it a valuable component in the formulation of these products, helping to protect crops and maintain agricultural productivity.
Used in Insecticides and Pest Control:
1-(2-Hydroxyphenyl)-3-(piperidino)-2-propene-1-one is used as an active ingredient in insecticides and pest control products due to its demonstrated effectiveness against various insects and mites. Its incorporation into these products helps to control and manage pest populations, reducing their impact on crops and the environment.
It is crucial to handle and use 1-(2-Hydroxyphenyl)-3-(piperidino)-2-propene-1-one with care, as it may pose potential health hazards and toxicity. Proper safety measures and guidelines should be followed to minimize risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 1084-62-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,8 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1084-62:
(6*1)+(5*0)+(4*8)+(3*4)+(2*6)+(1*2)=64
64 % 10 = 4
So 1084-62-4 is a valid CAS Registry Number.

1084-62-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-hydroxy-phenyl)-3-piperidin-1-yl-propenone

1.2 Other means of identification

Product number -
Other names 1-[2-(2-hydroxybenzoyl)ethenyl]piperidine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1084-62-4 SDS

1084-62-4Downstream Products

1084-62-4Relevant articles and documents

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

Dalvi,Shelke,Karale,Gill

, p. 1421 - 1424 (2007)

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

Sugita, Yoshiaki,Iwaki, Takako,Okamoto, Misaki,Yokoe, Ichiro

, p. 881 - 888 (2007/10/03)

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

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