tert-Butyl (2-oxo-3-(trifluoromethyl)piperidin-3-yl)carbamate

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Reagent Code: #130623
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CAS Number 195196-07-7

science Other reagents with same CAS 195196-07-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 282.26 g/mol
Formula C₁₁H₁₇F₃N₂O₃
badge Registry Numbers
MDL Number MFCD07779909
thermostat Physical Properties
Boiling Point 390.6±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.25±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules targeting central nervous system disorders. Its structure supports the construction of complex heterocyclic systems found in experimental therapeutics, including those with potential antipsychotic or antidepressant activity. The tert-butyl carbamate group serves as a protecting group for amines during multi-step syntheses, enabling selective reactions. Additionally, the presence of the trifluoromethyl moiety enhances metabolic stability and lipophilicity, which are desirable traits in drug design. Commonly employed in medicinal chemistry research for scaffold modification and structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿17,650.00
inventory 250mg
10-20 days ฿29,990.00

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tert-Butyl (2-oxo-3-(trifluoromethyl)piperidin-3-yl)carbamate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules targeting central nervous system disorders. Its structure supports the construction of complex heterocyclic systems found in experimental therapeutics, including those with potential antipsychotic or antidepressant activity. The tert-butyl carbamate group serves as a protecting group for amines during multi-step syntheses, enabling selective reactions. Additionally, the presence of

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules targeting central nervous system disorders. Its structure supports the construction of complex heterocyclic systems found in experimental therapeutics, including those with potential antipsychotic or antidepressant activity. The tert-butyl carbamate group serves as a protecting group for amines during multi-step syntheses, enabling selective reactions. Additionally, the presence of the trifluoromethyl moiety enhances metabolic stability and lipophilicity, which are desirable traits in drug design. Commonly employed in medicinal chemistry research for scaffold modification and structure-activity relationship studies.

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