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N-[4-(2-Fluoroethoxy)phenyl]acetamide is a chemical compound with the molecular formula C10H12FNO2. It is an amide derivative, characterized by the presence of an amide functional group (-CONH2) attached to a phenyl ring. The phenyl ring has a fluoroethoxy group (-OCH2CH2F) at the 4-position, which introduces a fluorine atom into the molecule. This fluoroalkyl group can significantly influence the compound's physical and chemical properties, such as solubility, reactivity, and bioavailability. The compound may be used in various applications, including pharmaceuticals, agrochemicals, or as intermediates in organic synthesis, due to its unique structure and potential to modulate molecular interactions.

714-24-9

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714-24-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 714-24-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 714-24:
(5*7)+(4*1)+(3*4)+(2*2)+(1*4)=59
59 % 10 = 9
So 714-24-9 is a valid CAS Registry Number.

714-24-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-acetamidophenyl 2-fluoroethyl ether

1.2 Other means of identification

Product number -
Other names -

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

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More Details:714-24-9 SDS

714-24-9Relevant academic research and scientific papers

Direct Deoxyfluorination of Alcohols with KF as the Fluorine Source

Xu, Jun,Peng, Chao,Yao, Bolin,Xu, Hua-Jian,Xie, Qiang

, p. 6471 - 6478 (2022/05/07)

This report describes a method for the deoxyfluorination of alcohols with KF as the fluorine source via in situ generation of highly active CF3SO2F. Diverse functionalities, including halogen, nitro, ketone, ester, alkene, and alkyne, are well tolerated. Mild conditions, a short reaction time, and a wide substrate scope make this method an excellent choice for the construction of C-F bonds.

Synthesis of an 18F-labelled high affinity β1- adrenoceptor PET radioligand based on ICI 89,406

Wagner, Stefan,Law, Marilyn P.,Riemann, Burkhard,Pike, Victor W.,Breyholz, Hans-Joerg,Hoeltke, Garsten,Faust, Andreas,Renner, Christiane,Schober, Otmar,Schaefers, Michael,Kopka, Klaus

, p. 177 - 195 (2007/10/03)

To date, some non-selective β-adrenoceptor (β-AR) positron emission tomography (PET) radioligands are in clinical use, but no PET radioligand for the selective imaging of cardiac β1-ARs is clinically available. Therefore, the aim of this study

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