5-[(tert-Butoxy)carbonyl]-4H,5H,6H,7H-[1,2]oxazolo[4,5-c]pyridine-3-carboxylic acid

≥95%

Reagent Code: #86765
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CAS Number 912265-93-1

science Other reagents with same CAS 912265-93-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 268.27 g/mol
Formula C₁₂H₁₆N₂O₅
badge Registry Numbers
MDL Number MFCD12198786
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

This chemical is primarily used in pharmaceutical research and development as a key intermediate in the synthesis of more complex molecules. Its structure makes it valuable for constructing heterocyclic compounds, which are often found in drugs targeting various diseases. It is particularly useful in medicinal chemistry for designing and optimizing drug candidates, especially those involving central nervous system (CNS) disorders or anti-inflammatory applications. Additionally, it serves as a building block in organic synthesis, enabling the creation of novel compounds with potential therapeutic properties. Its tert-butoxycarbonyl (Boc) protecting group allows for selective reactions, making it a versatile tool in multi-step synthetic processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,190.00

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5-[(tert-Butoxy)carbonyl]-4H,5H,6H,7H-[1,2]oxazolo[4,5-c]pyridine-3-carboxylic acid
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This chemical is primarily used in pharmaceutical research and development as a key intermediate in the synthesis of more complex molecules. Its structure makes it valuable for constructing heterocyclic compounds, which are often found in drugs targeting various diseases. It is particularly useful in medicinal chemistry for designing and optimizing drug candidates, especially those involving central nervous system (CNS) disorders or anti-inflammatory applications. Additionally, it serves as a building block in organic synthesis, enabling the creation of novel compounds with potential therapeutic properties. Its tert-butoxycarbonyl (Boc) protecting group allows for selective reactions, making it a versatile tool in multi-step synthetic processes.
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