rel-tert-Butyl ((1R,2S)-2-fluorocyclopropyl)carbamate

95%

Reagent Code: #82789
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CAS Number 105919-35-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 175.20 g/mol
Formula C₈H₁₄FNO₂
badge Registry Numbers
MDL Number MFCD18835705
thermostat Physical Properties
Boiling Point 238.4±29.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.09±0.1 g/cm3(Predicted)
Storage room temperature

description Product Description

This compound is primarily utilized in the pharmaceutical and medicinal chemistry fields as a key intermediate in the synthesis of more complex molecules. Its structure, featuring a fluorinated cyclopropyl group and a tert-butyl carbamate moiety, makes it valuable for designing and developing bioactive compounds, particularly those targeting enzymes or receptors where fluorine substitution can enhance binding affinity or metabolic stability. It is often employed in the preparation of potential drug candidates, especially in the development of antiviral, anticancer, or anti-inflammatory agents. Additionally, its stereochemistry and functional groups allow for precise modifications in drug discovery programs, enabling researchers to fine-tune pharmacological properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days $657.55
inventory 250mg
10-20 days $1,315.10
rel-tert-Butyl ((1R,2S)-2-fluorocyclopropyl)carbamate
This compound is primarily utilized in the pharmaceutical and medicinal chemistry fields as a key intermediate in the synthesis of more complex molecules. Its structure, featuring a fluorinated cyclopropyl group and a tert-butyl carbamate moiety, makes it valuable for designing and developing bioactive compounds, particularly those targeting enzymes or receptors where fluorine substitution can enhance binding affinity or metabolic stability. It is often employed in the preparation of potential drug candidates, especially in the development of antiviral, anticancer, or anti-inflammatory agents. Additionally, its stereochemistry and functional groups allow for precise modifications in drug discovery programs, enabling researchers to fine-tune pharmacological properties.
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