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AA33984

120136-28-9 | Benzene, 4-ethynyl-2-fluoro-1-methoxy-

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $120.00 $84.00 -   +
250mg 95% in stock $225.00 $158.00 -   +
1g 95% in stock $457.00 $320.00 -   +
5g 95% in stock $1,567.00 $1,097.00 -   +
10g 95% in stock $2,499.00 $1,749.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA33984
Chemical Name: Benzene, 4-ethynyl-2-fluoro-1-methoxy-
CAS Number: 120136-28-9
Molecular Formula: C9H7FO
Molecular Weight: 150.1497
MDL Number: MFCD08703468
SMILES: C#Cc1ccc(c(c1)F)OC

 

Upstream Synthesis Route
  • 4-Ethynyl-2-fluoro-1-methoxybenzene, also known as $name$, is a versatile compound that finds widespread application in chemical synthesis. Its unique structure, characterized by the presence of both ethynyl and fluoro functional groups, imparts specific properties that make it a valuable building block for various organic reactions.In chemical synthesis, $name$ serves as a key reagent for the introduction of the ethynyl group into organic molecules. The ethynyl moiety, a reactive alkyne group, can participate in various coupling reactions such as Sonogashira coupling, allowing for the formation of carbon-carbon bonds. This capability makes $name$ useful for the construction of complex organic frameworks, particularly in the development of pharmaceuticals, agrochemicals, and materials science.Additionally, the presence of the fluoro and methoxy groups in $name$ adds another layer of versatility. The fluoro group can act as a directing group in transition metal-catalyzed reactions, facilitating selective functionalization at specific positions within a molecule. The methoxy group, on the other hand, can serve as a protecting group or provide steric hindrance to control the regioselectivity of reactions.Overall, the strategic placement of the ethynyl, fluoro, and methoxy functionalities in 4-Ethynyl-2-fluoro-1-methoxybenzene makes it a valuable tool for chemists engaged in organic synthesis. Its ability to participate in diverse chemical transformations underscores its importance in the creation of novel compounds with tailored properties for a range of applications.
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