N-Boc-5-Hydroxyindole

95%

Reagent Code: #217266
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CAS Number 434958-85-7

science Other reagents with same CAS 434958-85-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.26 g/mol
Formula C₁₃H₁₅NO₃
thermostat Physical Properties
Boiling Point 374.5°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Widely used in pharmaceutical synthesis, particularly in the production of serotonin-related compounds and tryptamine derivatives. Its free hydroxyl group and protected indole nitrogen functionalities make it ideal for selective reactions in multi-step organic syntheses. Commonly employed in the development of central nervous system agents, including antidepressants and antipsychotics. The Boc group allows for easy deprotection under mild acidic conditions, enabling efficient chain elongation or cyclization in drug discovery. Also utilized in the preparation of natural product analogs and bioactive molecules requiring indole scaffolds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿700.00
inventory 1g
10-20 days ฿2,090.00
inventory 5g
10-20 days ฿10,310.00

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N-Boc-5-Hydroxyindole
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Widely used in pharmaceutical synthesis, particularly in the production of serotonin-related compounds and tryptamine derivatives. Its free hydroxyl group and protected indole nitrogen functionalities make it ideal for selective reactions in multi-step organic syntheses. Commonly employed in the development of central nervous system agents, including antidepressants and antipsychotics. The Boc group allows for easy deprotection under mild acidic conditions, enabling efficient chain elongation or cyclizat

Widely used in pharmaceutical synthesis, particularly in the production of serotonin-related compounds and tryptamine derivatives. Its free hydroxyl group and protected indole nitrogen functionalities make it ideal for selective reactions in multi-step organic syntheses. Commonly employed in the development of central nervous system agents, including antidepressants and antipsychotics. The Boc group allows for easy deprotection under mild acidic conditions, enabling efficient chain elongation or cyclization in drug discovery. Also utilized in the preparation of natural product analogs and bioactive molecules requiring indole scaffolds.

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