Carbonic acid, (1R,2S)-2-[(2,2-dichloroacetyl)amino]-3-fluoro-1-[4-(methylsulfonyl)phenyl]propyl 3-methylbutylester

95%

Reagent Code: #54477
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CAS Number 943591-86-4

science Other reagents with same CAS 943591-86-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 472.36 g/mol
Formula C₁₈H₂₄Cl₂FNO₆S
thermostat Physical Properties
Boiling Point 625.0±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.317±0.06 g/cm3(Predicted)
Storage 2-8℃

description Product Description

This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of more complex molecules. Its structure, featuring a fluorinated phenyl group and a dichloroacetyl moiety, makes it valuable in the development of biologically active compounds, particularly those targeting specific enzymes or receptors. It is often employed in research focused on creating new therapeutic agents, especially in areas like anti-inflammatory or anticancer drug development. Additionally, its unique chemical properties may be explored in the design of prodrugs, where it could enhance drug delivery or improve bioavailability. In laboratory settings, it serves as a key building block for organic synthesis, aiding in the creation of novel chemical entities for further pharmacological evaluation.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿21,600.00

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Carbonic acid, (1R,2S)-2-[(2,2-dichloroacetyl)amino]-3-fluoro-1-[4-(methylsulfonyl)phenyl]propyl 3-methylbutylester
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This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of more complex molecules. Its structure, featuring a fluorinated phenyl group and a dichloroacetyl moiety, makes it valuable in the development of biologically active compounds, particularly those targeting specific enzymes or receptors. It is often employed in research focused on creating new therapeutic agents, especially in areas like anti-inflammatory or anticancer drug development. Additionally, its unique chemical properties may be explored in the design of prodrugs, where it could enhance drug delivery or improve bioavailability. In laboratory settings, it serves as a key building block for organic synthesis, aiding in the creation of novel chemical entities for further pharmacological evaluation.
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