tert-Butyl 3-(hydroxymethyl)-7-nitro-1H-indole-1-carboxylate

≥95%

Reagent Code: #114547
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CAS Number 914349-15-8

science Other reagents with same CAS 914349-15-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 292.29 g/mol
Formula C₁₄H₁₆N₂O₅
badge Registry Numbers
MDL Number MFCD05864725
thermostat Physical Properties
Boiling Point 470.2°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in organic synthesis and medicinal chemistry research. It serves as a key intermediate in the development of indole-based pharmaceuticals, particularly in the synthesis of compounds with potential biological activity. Its structure, featuring a nitro group and a hydroxylmethyl group, makes it a versatile building block for modifying indole derivatives, which are often explored for their therapeutic properties. Researchers use it to create novel molecules for drug discovery, especially in areas like anti-inflammatory, anticancer, and antimicrobial agents. Additionally, it can be employed in the study of enzyme inhibitors or receptor modulators due to its reactive functional groups.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,392.00
inventory 10g
10-20 days ฿24,966.00
inventory 5g
10-20 days ฿16,632.00
inventory 250mg
10-20 days ฿1,773.00

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tert-Butyl 3-(hydroxymethyl)-7-nitro-1H-indole-1-carboxylate
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This compound is primarily utilized in organic synthesis and medicinal chemistry research. It serves as a key intermediate in the development of indole-based pharmaceuticals, particularly in the synthesis of compounds with potential biological activity. Its structure, featuring a nitro group and a hydroxylmethyl group, makes it a versatile building block for modifying indole derivatives, which are often explored for their therapeutic properties. Researchers use it to create novel molecules for drug disco

This compound is primarily utilized in organic synthesis and medicinal chemistry research. It serves as a key intermediate in the development of indole-based pharmaceuticals, particularly in the synthesis of compounds with potential biological activity. Its structure, featuring a nitro group and a hydroxylmethyl group, makes it a versatile building block for modifying indole derivatives, which are often explored for their therapeutic properties. Researchers use it to create novel molecules for drug discovery, especially in areas like anti-inflammatory, anticancer, and antimicrobial agents. Additionally, it can be employed in the study of enzyme inhibitors or receptor modulators due to its reactive functional groups.

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