Methyl 6-((tert-butoxycarbonyl)amino)-3-formyl-1H-indole-4-carboxylate

≥95%

Reagent Code: #208662
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CAS Number 731810-57-4

science Other reagents with same CAS 731810-57-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 318.33 g/mol
Formula C₁₆H₁₈N₂O₅
badge Registry Numbers
MDL Number MFCD09800496
thermostat Physical Properties
Boiling Point 473.5°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.323g/cm3
Storage 2-8°C, stored in inert gas

description Product Description

Used in pharmaceutical synthesis as an intermediate for developing bioactive molecules, particularly in the production of indole-based drug candidates. Its functional groups—aldehyde, ester, and protected amine—allow selective reactions for building complex structures, especially in anticancer and antiviral research. Commonly employed in medicinal chemistry for constructing tryptamine or tryptophan derivatives through multi-step synthesis. The Boc-protected amine ensures stability during reactions, while the aldehyde enables coupling or cyclization steps, making it valuable in heterocyclic compound development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,090.00
inventory 250mg
10-20 days ฿8,170.00

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Methyl 6-((tert-butoxycarbonyl)amino)-3-formyl-1H-indole-4-carboxylate
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Used in pharmaceutical synthesis as an intermediate for developing bioactive molecules, particularly in the production of indole-based drug candidates. Its functional groups—aldehyde, ester, and protected amine—allow selective reactions for building complex structures, especially in anticancer and antiviral research. Commonly employed in medicinal chemistry for constructing tryptamine or tryptophan derivatives through multi-step synthesis. The Boc-protected amine ensures stability during reactions, while

Used in pharmaceutical synthesis as an intermediate for developing bioactive molecules, particularly in the production of indole-based drug candidates. Its functional groups—aldehyde, ester, and protected amine—allow selective reactions for building complex structures, especially in anticancer and antiviral research. Commonly employed in medicinal chemistry for constructing tryptamine or tryptophan derivatives through multi-step synthesis. The Boc-protected amine ensures stability during reactions, while the aldehyde enables coupling or cyclization steps, making it valuable in heterocyclic compound development.

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