(E)-Ethyl 4-((tert-butoxycarbonyl)(methyl)amino)but-2-enoate

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Reagent Code: #113405
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CAS Number 149650-08-8

science Other reagents with same CAS 149650-08-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.3 g/mol
Formula C₁₂H₂₁NO₄
badge Registry Numbers
MDL Number MFCD30472003
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and an ethyl ester, makes it valuable in peptide synthesis and the development of pharmaceuticals. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization of the molecule. Additionally, the ethyl ester moiety can undergo hydrolysis or transesterification reactions, providing flexibility in synthetic routes. It is particularly useful in the synthesis of β-amino acids and their derivatives, which are important building blocks in medicinal chemistry. The compound’s conjugated double bond also enables it to participate in various cycloaddition reactions, expanding its utility in the construction of heterocyclic compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,208.00
inventory 250mg
10-20 days ฿13,941.00
inventory 1g
10-20 days ฿37,620.00

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(E)-Ethyl 4-((tert-butoxycarbonyl)(methyl)amino)but-2-enoate
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This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and an ethyl ester, makes it valuable in peptide synthesis and the development of pharmaceuticals. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization of the molecule. Additionally, the ethyl ester moiety can undergo hydrolysis or transesterifi

This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and an ethyl ester, makes it valuable in peptide synthesis and the development of pharmaceuticals. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization of the molecule. Additionally, the ethyl ester moiety can undergo hydrolysis or transesterification reactions, providing flexibility in synthetic routes. It is particularly useful in the synthesis of β-amino acids and their derivatives, which are important building blocks in medicinal chemistry. The compound’s conjugated double bond also enables it to participate in various cycloaddition reactions, expanding its utility in the construction of heterocyclic compounds.

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