tert-Butyl 3-(hydroxymethyl)-6-methyl-1H-indole-1-carboxylate

95%

Reagent Code: #146154
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CAS Number 914349-04-5

science Other reagents with same CAS 914349-04-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 261.32 g/mol
Formula C₁₅H₁₉NO₃
badge Registry Numbers
MDL Number MFCD05864708
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and other central nervous system (CNS) active agents. Its indole core structure is common in bioactive molecules, making it valuable in medicinal chemistry for constructing drug candidates targeting neurological disorders. The tert-butyl carbamate (Boc) group provides protection during multi-step syntheses, allowing selective reactions at other functional sites. The hydroxymethyl and methyl substituents enhance structural diversity and can influence binding affinity and metabolic stability in final drug compounds. Commonly employed in research settings for generating analogs in structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿700.00
inventory 1g
10-20 days ฿1,490.00

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tert-Butyl 3-(hydroxymethyl)-6-methyl-1H-indole-1-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and other central nervous system (CNS) active agents. Its indole core structure is common in bioactive molecules, making it valuable in medicinal chemistry for constructing drug candidates targeting neurological disorders. The tert-butyl carbamate (Boc) group provides protection during multi-step syntheses, allowing selective reactions at other functional sites. The hydroxymeth

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and other central nervous system (CNS) active agents. Its indole core structure is common in bioactive molecules, making it valuable in medicinal chemistry for constructing drug candidates targeting neurological disorders. The tert-butyl carbamate (Boc) group provides protection during multi-step syntheses, allowing selective reactions at other functional sites. The hydroxymethyl and methyl substituents enhance structural diversity and can influence binding affinity and metabolic stability in final drug compounds. Commonly employed in research settings for generating analogs in structure-activity relationship (SAR) studies.

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