5-Ethynyl-2-fluorobenzaldehyde

97%

Reagent Code: #184761
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CAS Number 1440535-11-4

science Other reagents with same CAS 1440535-11-4

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Weight 148.14 g/mol
Formula C₉H₅FO
badge Registry Numbers
MDL Number MFCD24850036
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its aldehyde and ethynyl functional groups allow for selective coupling reactions, such as Sonogashira and Wittig reactions, enabling the construction of complex molecular architectures. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance binding affinity and metabolic stability in drug candidates. Also utilized in the preparation of fluorescent probes and bioconjugates for imaging and diagnostic applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,980.00
inventory 250mg
10-20 days ฿5,540.00
inventory 1g
10-20 days ฿15,430.00

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5-Ethynyl-2-fluorobenzaldehyde
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its aldehyde and ethynyl functional groups allow for selective coupling reactions, such as Sonogashira and Wittig reactions, enabling the construction of complex molecular architectures. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance binding affinity and metabolic stability in drug cand

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its aldehyde and ethynyl functional groups allow for selective coupling reactions, such as Sonogashira and Wittig reactions, enabling the construction of complex molecular architectures. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance binding affinity and metabolic stability in drug candidates. Also utilized in the preparation of fluorescent probes and bioconjugates for imaging and diagnostic applications.

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