(S)-Methyl 2-((tert-butoxycarbonyl)amino)-3,3-dimethylbutanoate

95%

Reagent Code: #38100
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CAS Number 176504-88-4

science Other reagents with same CAS 176504-88-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.32 g/mol
Formula C₁₂H₂₃NO₄
badge Registry Numbers
MDL Number MFCD11113188
thermostat Physical Properties
Boiling Point 317.3°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily used in organic synthesis as a building block for the preparation of more complex molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the synthesis of peptides and peptidomimetics, where the tert-butoxycarbonyl (Boc) group acts as a protective group for amines during multi-step reactions. Its chiral structure makes it valuable in the production of enantiomerically pure compounds, which are essential for drug development. Additionally, it is utilized in research for designing and synthesizing bioactive compounds, including enzyme inhibitors and receptor ligands, due to its stability and ease of modification.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿585.00
inventory 1g
10-20 days ฿2,097.00
inventory 250mg
10-20 days ฿828.00

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(S)-Methyl 2-((tert-butoxycarbonyl)amino)-3,3-dimethylbutanoate
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This chemical is primarily used in organic synthesis as a building block for the preparation of more complex molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the synthesis of peptides and peptidomimetics, where the tert-butoxycarbonyl (Boc) group acts as a protective group for amines during multi-step reactions. Its chiral structure makes it valuable in the production of enantiomerically pure compounds, which are essential for drug development. Additionally, it is utilized in research for designing and synthesizing bioactive compounds, including enzyme inhibitors and receptor ligands, due to its stability and ease of modification.
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