137266-00-3 Usage
Uses
Used in Pharmaceutical Industry:
Ethanone, 1-[2-[(2-bromo-2-propenyl)oxy]phenyl]is used as a key intermediate in the synthesis of various pharmaceutical compounds due to its unique structure and reactivity, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, Ethanone, 1-[2-[(2-bromo-2-propenyl)oxy]phenyl]serves as an essential intermediate for the production of agrochemicals, including pesticides and herbicides, leveraging its chemical properties to enhance the effectiveness of these products.
Used in Organic Synthesis:
Ethanone, 1-[2-[(2-bromo-2-propenyl)oxy]phenyl]is utilized as a versatile building block in organic synthesis, enabling the creation of a wide range of organic compounds for various applications across different industries.
Used in Research and Development:
This chemical compound is also employed in research and development settings to explore its potential biological and pharmacological properties, with the aim of uncovering new applications and understanding its mechanisms of action.
Check Digit Verification of cas no
The CAS Registry Mumber 137266-00-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,2,6 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 137266-00:
(8*1)+(7*3)+(6*7)+(5*2)+(4*6)+(3*6)+(2*0)+(1*0)=123
123 % 10 = 3
So 137266-00-3 is a valid CAS Registry Number.
137266-00-3Relevant academic research and scientific papers
Intramolecular Addition of Vinyl and Aryl Radicals to Oxime Ethers in the Synthesis of Five-, Six- and Seven-membered Ring Systems
Booth, Susan E.,Jenkins, Paul R.,Swain, Christopher J.,Sweeney, Joseph B.
, p. 3499 - 3508 (2007/10/02)
The oxime ethers 2a-e have been cyclised with Bu3SnH to the alkoxyamino-3-methylidenechromanes 3a-e.Seven-membered ring formation was observed when the oxime ethers 7a, b were converted into the dibenzooxepines 8a, b under similar conditions. 1-Metho
