Methyl 2-(azetidin-3-yl)acetate 2,2,2-trifluoroacetate

95%

Reagent Code: #41980
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CAS Number 1313738-62-3

science Other reagents with same CAS 1313738-62-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.18 g/mol
Formula C₈H₁₂F₃NO₄
badge Registry Numbers
MDL Number MFCD18425634
inventory_2 Storage & Handling
Storage 2-8℃, inert gas

description Product Description

This compound is primarily utilized in organic synthesis and pharmaceutical research as a building block for the development of more complex molecules. Its structure, featuring an azetidine ring and a trifluoroacetate group, makes it valuable in the creation of biologically active compounds, particularly those targeting neurological disorders or acting as enzyme inhibitors. The trifluoroacetate moiety enhances its reactivity, facilitating its use in peptide coupling reactions and other chemical transformations. Additionally, it serves as an intermediate in the synthesis of drugs with potential applications in treating conditions like hypertension, anxiety, or pain management. Its versatility in medicinal chemistry underscores its importance in drug discovery and development.

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Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿16,992.00
inventory 5g
10-20 days ฿9,837.00
inventory 1g
10-20 days ฿2,889.00

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Methyl 2-(azetidin-3-yl)acetate 2,2,2-trifluoroacetate
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This compound is primarily utilized in organic synthesis and pharmaceutical research as a building block for the development of more complex molecules. Its structure, featuring an azetidine ring and a trifluoroacetate group, makes it valuable in the creation of biologically active compounds, particularly those targeting neurological disorders or acting as enzyme inhibitors. The trifluoroacetate moiety enhances its reactivity, facilitating its use in peptide coupling reactions and other chemical transform

This compound is primarily utilized in organic synthesis and pharmaceutical research as a building block for the development of more complex molecules. Its structure, featuring an azetidine ring and a trifluoroacetate group, makes it valuable in the creation of biologically active compounds, particularly those targeting neurological disorders or acting as enzyme inhibitors. The trifluoroacetate moiety enhances its reactivity, facilitating its use in peptide coupling reactions and other chemical transformations. Additionally, it serves as an intermediate in the synthesis of drugs with potential applications in treating conditions like hypertension, anxiety, or pain management. Its versatility in medicinal chemistry underscores its importance in drug discovery and development.

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