(S)-tert-Butyl 2-(2,2,2-trifluoroacetyl)pyrrolidine-1-carboxylate

95%

Reagent Code: #38118
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CAS Number 913979-70-1

science Other reagents with same CAS 913979-70-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 267.2449 g/mol
Formula C₁₁H₁₆F₃NO₃
badge Registry Numbers
MDL Number MFCD22570647
inventory_2 Storage & Handling
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description Product Description

This compound is primarily used in organic synthesis as a chiral building block or intermediate in the production of pharmaceuticals and fine chemicals. Its structure, featuring a pyrrolidine ring and a trifluoroacetyl group, makes it valuable for introducing chirality and fluorine atoms into target molecules. It is often employed in the synthesis of bioactive compounds, particularly in the development of drugs targeting neurological disorders, cardiovascular diseases, and other therapeutic areas. The tert-butyloxycarbonyl (Boc) protecting group enhances its stability during synthetic processes, allowing for selective reactions and easier purification. Additionally, its trifluoroacetyl moiety can serve as a precursor for further functionalization, making it a versatile reagent in medicinal chemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,329.00
inventory 5g
10-20 days ฿95,320.00

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(S)-tert-Butyl 2-(2,2,2-trifluoroacetyl)pyrrolidine-1-carboxylate
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This compound is primarily used in organic synthesis as a chiral building block or intermediate in the production of pharmaceuticals and fine chemicals. Its structure, featuring a pyrrolidine ring and a trifluoroacetyl group, makes it valuable for introducing chirality and fluorine atoms into target molecules. It is often employed in the synthesis of bioactive compounds, particularly in the development of drugs targeting neurological disorders, cardiovascular diseases, and other therapeutic areas. The te

This compound is primarily used in organic synthesis as a chiral building block or intermediate in the production of pharmaceuticals and fine chemicals. Its structure, featuring a pyrrolidine ring and a trifluoroacetyl group, makes it valuable for introducing chirality and fluorine atoms into target molecules. It is often employed in the synthesis of bioactive compounds, particularly in the development of drugs targeting neurological disorders, cardiovascular diseases, and other therapeutic areas. The tert-butyloxycarbonyl (Boc) protecting group enhances its stability during synthetic processes, allowing for selective reactions and easier purification. Additionally, its trifluoroacetyl moiety can serve as a precursor for further functionalization, making it a versatile reagent in medicinal chemistry and drug discovery.

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