Methyl 2-((tert-butoxycarbonyl)(methyl)amino)acetate

≥95%

Reagent Code: #41170
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CAS Number 42492-57-9

science Other reagents with same CAS 42492-57-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.24 g/mol
Formula C₉H₁₇NO₄
badge Registry Numbers
MDL Number MFCD04973115
thermostat Physical Properties
Boiling Point 249.6°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in organic synthesis as a building block for the preparation of more complex molecules. It serves as a key intermediate in the synthesis of peptides and peptidomimetics, where it aids in the protection of amino groups during multi-step reactions. The tert-butoxycarbonyl (Boc) group acts as a protective moiety, ensuring selective reactivity in the presence of other functional groups. Additionally, it is employed in the development of pharmaceuticals, particularly in the creation of active pharmaceutical ingredients (APIs) that require controlled introduction of nitrogen-containing structures. Its ester functionality also makes it a versatile precursor for further chemical modifications, such as hydrolysis or reduction, to yield desired products for various applications in medicinal chemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,178.00
inventory 250mg
10-20 days ฿333.00
inventory 25g
10-20 days ฿9,162.00
inventory 1g
10-20 days ฿531.00

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Methyl 2-((tert-butoxycarbonyl)(methyl)amino)acetate
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This compound is primarily utilized in organic synthesis as a building block for the preparation of more complex molecules. It serves as a key intermediate in the synthesis of peptides and peptidomimetics, where it aids in the protection of amino groups during multi-step reactions. The tert-butoxycarbonyl (Boc) group acts as a protective moiety, ensuring selective reactivity in the presence of other functional groups. Additionally, it is employed in the development of pharmaceuticals, particularly in the

This compound is primarily utilized in organic synthesis as a building block for the preparation of more complex molecules. It serves as a key intermediate in the synthesis of peptides and peptidomimetics, where it aids in the protection of amino groups during multi-step reactions. The tert-butoxycarbonyl (Boc) group acts as a protective moiety, ensuring selective reactivity in the presence of other functional groups. Additionally, it is employed in the development of pharmaceuticals, particularly in the creation of active pharmaceutical ingredients (APIs) that require controlled introduction of nitrogen-containing structures. Its ester functionality also makes it a versatile precursor for further chemical modifications, such as hydrolysis or reduction, to yield desired products for various applications in medicinal chemistry and drug discovery.

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