3-AMINOMETHYL-INDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

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Reagent Code: #44535
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CAS Number 188988-46-7

science Other reagents with same CAS 188988-46-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.3 g/mol
Formula C₁₄H₁₈N₂O₂
badge Registry Numbers
MDL Number MFCD06738803
inventory_2 Storage & Handling
Density 1.14±0.1 g/cm3(Predicted)
Storage 2-8℃

description Product Description

This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of more complex molecules, particularly in pharmaceutical research. It serves as a building block for the development of indole-based compounds, which are often explored for their biological activities, including potential therapeutic applications. Its tert-butyl ester group provides stability and facilitates selective reactions, making it valuable in multi-step synthetic processes. Additionally, it is used in the study of enzyme inhibitors and receptor modulators, contributing to drug discovery efforts.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿21,996.00
inventory 250mg
10-20 days ฿9,036.00

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3-AMINOMETHYL-INDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
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This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of more complex molecules, particularly in pharmaceutical research. It serves as a building block for the development of indole-based compounds, which are often explored for their biological activities, including potential therapeutic applications. Its tert-butyl ester group provides stability and facilitates selective reactions, making it valuable in multi-step synthetic processes. Additionally, it is used

This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of more complex molecules, particularly in pharmaceutical research. It serves as a building block for the development of indole-based compounds, which are often explored for their biological activities, including potential therapeutic applications. Its tert-butyl ester group provides stability and facilitates selective reactions, making it valuable in multi-step synthetic processes. Additionally, it is used in the study of enzyme inhibitors and receptor modulators, contributing to drug discovery efforts.

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