4-fluoro-2-(hex-1-yn-1-yl)benzaldehyde

95%

Reagent Code: #46693
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CAS Number 1207290-13-8

science Other reagents with same CAS 1207290-13-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.09 g/mol
Formula C₁₃H₁₃FO
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical is primarily utilized in organic synthesis as a versatile intermediate for constructing complex molecules. It is particularly valuable in the development of pharmaceuticals, where its aldehyde and alkyne functional groups enable diverse reactions such as cyclizations, coupling reactions, and the formation of heterocycles. Its fluorine substituent enhances the metabolic stability and binding affinity of the resulting compounds, making it useful in drug discovery for targeting specific biological pathways. Additionally, it finds applications in material science for synthesizing fluorinated aromatic compounds with unique electronic properties, which are essential in the production of advanced polymers and optoelectronic materials.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿5,967.00
5g
10-20 days ฿25,632.00
250mg
10-20 days ฿3,402.00

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4-fluoro-2-(hex-1-yn-1-yl)benzaldehyde
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This chemical is primarily utilized in organic synthesis as a versatile intermediate for constructing complex molecules. It is particularly valuable in the development of pharmaceuticals, where its aldehyde and alkyne functional groups enable diverse reactions such as cyclizations, coupling reactions, and the formation of heterocycles. Its fluorine substituent enhances the metabolic stability and binding affinity of the resulting compounds, making it useful in drug discovery for targeting specific biolog

This chemical is primarily utilized in organic synthesis as a versatile intermediate for constructing complex molecules. It is particularly valuable in the development of pharmaceuticals, where its aldehyde and alkyne functional groups enable diverse reactions such as cyclizations, coupling reactions, and the formation of heterocycles. Its fluorine substituent enhances the metabolic stability and binding affinity of the resulting compounds, making it useful in drug discovery for targeting specific biological pathways. Additionally, it finds applications in material science for synthesizing fluorinated aromatic compounds with unique electronic properties, which are essential in the production of advanced polymers and optoelectronic materials.

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