2-(1-(tert-Butoxycarbonyl)azepan-4-yl)acetic acid

95%

Reagent Code: #62295
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CAS Number 1268521-78-3

science Other reagents with same CAS 1268521-78-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.33 g/mol
Formula C₁₃H₂₃NO₄
badge Registry Numbers
MDL Number MFCD18633020
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily used in the synthesis of pharmaceutical compounds, particularly in the development of peptidomimetics and other bioactive molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and an azepane ring, makes it valuable in organic synthesis for constructing complex molecules. It is often employed in medicinal chemistry to create intermediates that can be further modified to produce potential drug candidates. Additionally, its carboxylic acid functionality allows for easy conjugation with other molecules, making it a versatile building block in drug discovery and development processes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿25,650.00

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2-(1-(tert-Butoxycarbonyl)azepan-4-yl)acetic acid
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This chemical is primarily used in the synthesis of pharmaceutical compounds, particularly in the development of peptidomimetics and other bioactive molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and an azepane ring, makes it valuable in organic synthesis for constructing complex molecules. It is often employed in medicinal chemistry to create intermediates that can be further modified to produce potential drug candidates. Additionally, its carboxylic acid functionality

This chemical is primarily used in the synthesis of pharmaceutical compounds, particularly in the development of peptidomimetics and other bioactive molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and an azepane ring, makes it valuable in organic synthesis for constructing complex molecules. It is often employed in medicinal chemistry to create intermediates that can be further modified to produce potential drug candidates. Additionally, its carboxylic acid functionality allows for easy conjugation with other molecules, making it a versatile building block in drug discovery and development processes.

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