tert-Butyl 7-(benzyloxy)-3-formyl-1H-indole-1-carboxylate

95%

Reagent Code: #146360
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CAS Number 914348-99-5

science Other reagents with same CAS 914348-99-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 351.4 g/mol
Formula C₂₁H₂₁NO₄
badge Registry Numbers
MDL Number MFCD05864703
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as a key intermediate in the synthesis of indole-based pharmaceuticals, particularly in the development of serotonin receptor modulators and anti-migraine agents. Its 3-formyl aldehyde, 7-benzyloxy protected hydroxyl, and N-1 tert-butoxycarbonyl (Boc) protecting group allow selective functionalization, enabling the construction of complex molecular architectures in medicinal chemistry. The Boc group protects the indole nitrogen during multi-step syntheses and can be deprotected under mild acidic conditions. Commonly employed in organic syntheses where controlled reactivity and stability are required.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,200.00
inventory 1g
10-20 days ฿2,890.00

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tert-Butyl 7-(benzyloxy)-3-formyl-1H-indole-1-carboxylate
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Used as a key intermediate in the synthesis of indole-based pharmaceuticals, particularly in the development of serotonin receptor modulators and anti-migraine agents. Its 3-formyl aldehyde, 7-benzyloxy protected hydroxyl, and N-1 tert-butoxycarbonyl (Boc) protecting group allow selective functionalization, enabling the construction of complex molecular architectures in medicinal chemistry. The Boc group protects the indole nitrogen during multi-step syntheses and can be deprotected under mild acidic con

Used as a key intermediate in the synthesis of indole-based pharmaceuticals, particularly in the development of serotonin receptor modulators and anti-migraine agents. Its 3-formyl aldehyde, 7-benzyloxy protected hydroxyl, and N-1 tert-butoxycarbonyl (Boc) protecting group allow selective functionalization, enabling the construction of complex molecular architectures in medicinal chemistry. The Boc group protects the indole nitrogen during multi-step syntheses and can be deprotected under mild acidic conditions. Commonly employed in organic syntheses where controlled reactivity and stability are required.

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