2-Fluoro-3-hydroxybenzamide

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Reagent Code: #42417
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CAS Number 951122-84-2

science Other reagents with same CAS 951122-84-2

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Weight 155.13 g/mol
Formula C₇H₆FNO₂
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Storage room temperature

description Product Description

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its structure is particularly valuable in developing drugs targeting neurological disorders, such as Alzheimer's disease, due to its ability to modulate specific enzyme activities. Additionally, it is explored in the creation of anti-inflammatory and analgesic agents, leveraging its unique fluorinated aromatic ring to enhance binding affinity and metabolic stability. Researchers also investigate its potential in designing novel antimicrobial compounds, given its structural compatibility with bacterial enzyme inhibition.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,213.00

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2-Fluoro-3-hydroxybenzamide
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Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its structure is particularly valuable in developing drugs targeting neurological disorders, such as Alzheimer's disease, due to its ability to modulate specific enzyme activities. Additionally, it is explored in the creation of anti-inflammatory and analgesic agents, leveraging its unique fluorinated aromatic ring to enhance binding affinity and metabolic stability. Rese

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its structure is particularly valuable in developing drugs targeting neurological disorders, such as Alzheimer's disease, due to its ability to modulate specific enzyme activities. Additionally, it is explored in the creation of anti-inflammatory and analgesic agents, leveraging its unique fluorinated aromatic ring to enhance binding affinity and metabolic stability. Researchers also investigate its potential in designing novel antimicrobial compounds, given its structural compatibility with bacterial enzyme inhibition.

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