2-(6-Methoxynaphthalen-2-yl)-2-methylpropanoicacid

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Reagent Code: #213570
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CAS Number 69337-85-5

science Other reagents with same CAS 69337-85-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.29 g/mol
Formula C₁₅H₁₆O₃
badge Registry Numbers
MDL Number MFCD01712996
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used primarily as a key intermediate in the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs), particularly naproxen. Its structure allows for efficient conversion into the active pharmaceutical ingredient through esterification or salt formation. It plays a critical role in enabling the chiral synthesis of (S)-naproxen, which is the therapeutically active enantiomer. The compound's stability and reactivity profile make it suitable for large-scale manufacturing processes in the pharmaceutical industry. Additionally, it is utilized in research settings for developing new derivatives with improved pharmacokinetic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,320.00
inventory 250mg
10-20 days ฿28,120.00
2-(6-Methoxynaphthalen-2-yl)-2-methylpropanoicacid
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Used primarily as a key intermediate in the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs), particularly naproxen. Its structure allows for efficient conversion into the active pharmaceutical ingredient through esterification or salt formation. It plays a critical role in enabling the chiral synthesis of (S)-naproxen, which is the therapeutically active enantiomer. The compound's stability and reactivity profile make it suitable for large-scale manufacturing processes in the pharmaceutical in

Used primarily as a key intermediate in the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs), particularly naproxen. Its structure allows for efficient conversion into the active pharmaceutical ingredient through esterification or salt formation. It plays a critical role in enabling the chiral synthesis of (S)-naproxen, which is the therapeutically active enantiomer. The compound's stability and reactivity profile make it suitable for large-scale manufacturing processes in the pharmaceutical industry. Additionally, it is utilized in research settings for developing new derivatives with improved pharmacokinetic properties.

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