Methyl 5-((tert-butoxycarbonyl)amino)-4-nitrothiophene-2-carboxylate

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Reagent Code: #48108
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CAS Number 1351238-59-9

science Other reagents with same CAS 1351238-59-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 302.30 g/mol
Formula C₁₁H₁₄N₂O₆S
badge Registry Numbers
MDL Number MFCD30833848
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed away from light

description Product Description

This chemical is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring both a nitro group and a tert-butoxycarbonyl (Boc) protected amine, makes it valuable in the development of pharmaceuticals and agrochemicals. The nitro group allows for further functionalization through reduction or substitution reactions, while the Boc group can be deprotected to reveal a free amine, enabling coupling reactions. It is particularly useful in the synthesis of thiophene-based compounds, which are often explored for their biological activities, such as antimicrobial, anti-inflammatory, or anticancer properties. Additionally, its ester group provides a handle for further chemical modifications, making it versatile in medicinal chemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,232.00
inventory 250mg
10-20 days ฿22,464.00

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Methyl 5-((tert-butoxycarbonyl)amino)-4-nitrothiophene-2-carboxylate
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This chemical is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring both a nitro group and a tert-butoxycarbonyl (Boc) protected amine, makes it valuable in the development of pharmaceuticals and agrochemicals. The nitro group allows for further functionalization through reduction or substitution reactions, while the Boc group can be deprotected to reveal a free amine, enabling coupling reactions. It is particularly useful in the synthesis of thiophene-based compounds, which are often explored for their biological activities, such as antimicrobial, anti-inflammatory, or anticancer properties. Additionally, its ester group provides a handle for further chemical modifications, making it versatile in medicinal chemistry and drug discovery.
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