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4′-Fluoroacetophenone CAS:403-42-9

4′-Fluoroacetophenone is an organic compound with the molecular formula C9H9F0. It features a phenyl group substituted by a fluoro group at the para position and an acetyl group attached to the benzene ring. This colorless to pale yellow liquid is known for its distinctive aroma and is commonly used in organic synthesis as an intermediate for pharmaceuticals, agrochemicals, and various fine chemicals. The presence of both the fluorine atom and the acetyl functional group imparts unique reactivity to 4′-fluoroacetophenone, making it valuable in chemical research and industrial applications.


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Application and Effect:

4'-Fluoroacetophenone is an aromatic ketone characterized by its structural components: a fluoro substituent at the para position of the acetophenone structure. Its molecular framework not only confers stability but also enhances its reactivity, offering numerous opportunities for chemical transformations. One of the primary applications of 4'-fluoroacetophenone is in the pharmaceutical industry, where it serves as an important intermediate for synthesizing various drugs. The introduction of the fluorine atom can significantly influence the biological activity and pharmacokinetics of drug candidates, contributing to enhanced potency and selectivity. Researchers often utilize 4'-fluoroacetophenone in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs) and other therapeutics. Additionally, 4'-fluoroacetophenone finds applications in the development of agrochemicals. The compound's ability to modify biological activity through fluorination allows for the design of effective pesticides and herbicides, which are essential for modern agricultural practices. By incorporating 4'-fluoroacetophenone into these formulations, chemists can enhance the efficacy and specificity of crop protection agents, thereby improving yield and sustainability in agricultural production. Moreover, in organic synthesis, 4'-fluoroacetophenone serves as a versatile building block for creating a wide range of complex molecules. It can undergo various reactions, such as nucleophilic substitutions and Friedel-Crafts acylations, allowing for the introduction of additional functional groups that expand its utility in chemical synthesis. This property is particularly advantageous in materials science, where it is employed to develop new polymers or advanced materials with tailored properties. The compound is also utilized in analytical chemistry as a reagent for the identification and quantification of certain substances. Its reactivity enables the formation of specific derivatives that can be analyzed using techniques such as chromatography and mass spectrometry, aiding in quality control and environmental monitoring. Synthesis of 4'-fluoroacetophenone typically involves the fluorination of acetophenone or its precursors, showcasing the practicality of this process in laboratory settings. The readily accessible nature of starting materials makes 4'-fluoroacetophenone a favored choice for researchers and chemists. While 4'-fluoroacetophenone possesses many beneficial applications, safety considerations must be taken into account when handling the compound. Proper protective measures, including gloves and eyewear, should be employed due to potential irritant properties. In conclusion, 4'-fluoroacetophenone plays a significant role in organic chemistry, contributing to advancements in pharmaceuticals, agrochemicals, and synthetic methodologies. Its unique chemical properties and versatility make it an essential compound in various scientific fields, reinforcing its relevance in contemporary research and industrial processes.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C8H7FO
Assay 99%
Appearance white powder
CAS No.  403-42-9
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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