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6437-63-4

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6437-63-4 Usage

General Description

1-(3-METHOXYPHENOXY)-2-PROPANONE, also known as 3-Methoxyphenoxyacetone, is a chemical compound with the formula C11H14O3. It is a ketone derivative with a propyl group attached to the carbonyl carbon and a 3-methoxyphenoxy group attached to the alpha carbon. 1-(3-METHOXYPHENOXY)-2-PROPANONE is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It has also been used as a reagent in the preparation of various compounds and is known for its ability to participate in a variety of chemical reactions. Additionally, it has been utilized in research as a building block for the development of new compounds with potential biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 6437-63-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,3 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6437-63:
(6*6)+(5*4)+(4*3)+(3*7)+(2*6)+(1*3)=104
104 % 10 = 4
So 6437-63-4 is a valid CAS Registry Number.

6437-63-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-methoxyphenoxy)propan-2-one

1.2 Other means of identification

Product number -
Other names 3-Methoxy-1-acetonyloxy-benzol

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:6437-63-4 SDS

6437-63-4Relevant articles and documents

Iridium-catalyzed enantioselective intramolecular hydroarylation of allylic aryl ethers devoid of a directing group on the aryl group

Kusaka, Satoshi,Ohmura, Toshimichi,Suginome, Michinori

supporting information, p. 13542 - 13545 (2021/12/23)

Although intramolecular hydroarylation is an attractive transformation of allylic aryl ethers, it has suffered from narrow substrate scope. We herein describe Ir/(S)-DTBM-SEGPHOS-catalyzed intramolecular hydroarylation of allylic aryl ethers. The reaction

BCl3-promoted synthesis of benzofurans

Kim, Ikyon,Lee, Sei-Hee,Lee, Sunkyung

body text, p. 6579 - 6584 (2009/04/06)

Lewis acidic nature of boron trichloride (BCl3) to coordinate to the carbonyl functionality was exploited for the synthesis of benzofurans via dehydrative cyclization. This mild and efficient procedure allowed for facile access to a number of h

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