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3'-Fluoro-4'-morpholinoacetophenone is a chemical compound characterized by the molecular formula C11H12FNO2. It is an acetophenone derivative featuring a fluorine atom at the 3' position and a morpholino group at the 4' position. 3'-Fluoro-4'-morpholinoacetophenone is recognized for its role in organic synthesis and medicinal chemistry, where it serves as a building block for creating a variety of biologically active molecules. Additionally, it has garnered interest for its potential pharmaceutical applications, particularly in the realms of anti-inflammatory and analgesic treatments. As a white crystalline solid with a melting point of approximately 40-42°C, 3'-Fluoro-4'-morpholinoacetophenone requires careful storage and handling due to its potentially hazardous properties.

189763-65-3

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189763-65-3 Usage

Uses

Used in Organic Synthesis:
3'-Fluoro-4'-morpholinoacetophenone is utilized as a key building block in organic synthesis for the creation of various biologically active molecules. Its unique structure, which includes a fluorine atom and a morpholino group, contributes to the diversity and reactivity of the compounds that can be synthesized from it.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 3'-Fluoro-4'-morpholinoacetophenone is employed as a precursor for the development of pharmaceuticals. Its structural features make it a valuable component in the design and synthesis of new drugs with potential therapeutic benefits.
Used in Pharmaceutical Applications:
3'-Fluoro-4'-morpholinoacetophenone is studied for its potential as an anti-inflammatory and analgesic agent. Its chemical properties and interactions with biological systems suggest that it may offer relief from inflammation and pain, making it a candidate for further research and development in the pharmaceutical industry.
Used in Research and Development:
3'-Fluoro-4'-morpholinoacetophenone is also used in research and development settings to explore its chemical properties and potential applications. The study of 3'-Fluoro-4'-morpholinoacetophenone aids in understanding its reactivity, stability, and interactions with other molecules, which can inform the design of new chemical processes and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 189763-65-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,7,6 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 189763-65:
(8*1)+(7*8)+(6*9)+(5*7)+(4*6)+(3*3)+(2*6)+(1*5)=203
203 % 10 = 3
So 189763-65-3 is a valid CAS Registry Number.

189763-65-3SDS

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 1-(3-Fluoro-4-morpholin-4-ylphenyl)ethanone

1.2 Other means of identification

Product number -
Other names 1-[3-fluoro-4-(morpholin-4-yl)phenyl]ethanone

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:189763-65-3 SDS

189763-65-3Downstream Products

189763-65-3Relevant academic research and scientific papers

6-PHENYL-4,5-DIHYDROPYRIDAZIN-3(2H)-ONE DERIVATIVES AS PDE3A AND PDE3B INHIBITORS FOR TREATING CANCER

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Page/Page column 157; 158, (2019/02/15)

The present invention provides 6-phenyl-4,5-dihydropyridazin-3(2H)- one derivatives of formula (I) : The present invention provides 6-phenyl-4,5-dihydropyridazin-3(2H)- one derivatives of formula (I) :

Silver-catalyzed intermolecular amination of fluoroarenes

Wang, Yu,Wei, Chenlong,Tang, Ruyun,Zhan, Haosheng,Lin, Jing,Liu, Zhenhua,Tao, Weihua,Fang, Zhongxue

supporting information, p. 6191 - 6194 (2018/09/10)

A novel highly selective Ag-catalyzed intermolecular amination of fluoroarenes has been developed. This transformation starts from readily available 4-carbonyl fluorobenzene and NaN3 or other nitrogen-source, via amination followed by C-F bond cleavage, thus affording the desired 4-carbonyl arylamine products under mild conditions. The reaction is accelerated using a small amount of water. This pathway is distinct from a previously reported radical amination reaction.

Compound capable of effectively inhibiting or killing multi-drug resistant bacteria and preparation method and application of compound

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Paragraph 0181; 0684, (2017/06/02)

The invention discloses a compound capable of effectively inhibiting or killing bacterial microorganisms. The compound has a structural general formula shown as the formula I (please see the formula in the description). Pharmacodynamic experiments prove that the compound can effectively inhibit or kill the broad-spectrum and multi-drug resistant staphylococcus aureus, streptococcus pneumoniae and staphylococcus aureus and is expected to be developed into a novel effective antibacterial drug with new targets.

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