1,1,1-trifluoro-N-[(1R,2R)-2-(trifluoromethylsulfonylamino)cyclohexyl]methanesulfonamide

98%

Reagent Code: #70174
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CAS Number 122833-60-7

science Other reagents with same CAS 122833-60-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 378.3123 g/mol
Formula C₈H₁₂F₆N₂O₄S₂
badge Registry Numbers
MDL Number MFCD01863491
thermostat Physical Properties
Melting Point 185-187 °C(lit.)
Boiling Point 345.849 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.64 g/cm3
Storage 2-8°C

description Product Description

This compound is primarily utilized in advanced chemical synthesis and pharmaceutical research due to its unique trifluoromethyl and sulfonamide functional groups. It serves as a key intermediate in the development of bioactive molecules, particularly in the creation of enzyme inhibitors and receptor antagonists. Its structural properties make it valuable in medicinal chemistry for designing drugs with enhanced metabolic stability and bioavailability. Additionally, it is employed in the study of chiral compounds, leveraging its stereochemistry to explore asymmetric synthesis pathways. Its applications also extend to material science, where it contributes to the development of specialized polymers and coatings with tailored properties.

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Test Parameter Specification
Appearance Solid
Purity (%) 97.5-100
Specific Rotation [A]20/D (C=5 In EtOH)(°) 3.1-9.1
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,888.00

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1,1,1-trifluoro-N-[(1R,2R)-2-(trifluoromethylsulfonylamino)cyclohexyl]methanesulfonamide
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This compound is primarily utilized in advanced chemical synthesis and pharmaceutical research due to its unique trifluoromethyl and sulfonamide functional groups. It serves as a key intermediate in the development of bioactive molecules, particularly in the creation of enzyme inhibitors and receptor antagonists. Its structural properties make it valuable in medicinal chemistry for designing drugs with enhanced metabolic stability and bioavailability. Additionally, it is employed in the study of chiral c

This compound is primarily utilized in advanced chemical synthesis and pharmaceutical research due to its unique trifluoromethyl and sulfonamide functional groups. It serves as a key intermediate in the development of bioactive molecules, particularly in the creation of enzyme inhibitors and receptor antagonists. Its structural properties make it valuable in medicinal chemistry for designing drugs with enhanced metabolic stability and bioavailability. Additionally, it is employed in the study of chiral compounds, leveraging its stereochemistry to explore asymmetric synthesis pathways. Its applications also extend to material science, where it contributes to the development of specialized polymers and coatings with tailored properties.

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