(1R,4r)-4-[(4-fluorobenzenesulfonamido)methyl]cyclohexane-1-carboxylic acid

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Reagent Code: #245764
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CAS Number 744248-54-2

science Other reagents with same CAS 744248-54-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 315.36 g/mol
Formula C₁₄H₁₈FNO₄S
thermostat Physical Properties
Boiling Point 489.2±51.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.319±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used in the synthesis of pharmaceutical agents, particularly as an intermediate in developing enzyme inhibitors. Its structure supports binding to specific biological targets, making it valuable in drug discovery for metabolic and inflammatory diseases. The compound's stereochemistry enhances selectivity in receptor interactions, improving efficacy and reducing side effects in final drug formulations. It is also employed in research settings to study structure-activity relationships in sulfonamide-based therapeutics.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿5,930.00
inventory 25mg
10-20 days ฿18,690.00
inventory 10mg
10-20 days ฿9,450.00

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(1R,4r)-4-[(4-fluorobenzenesulfonamido)methyl]cyclohexane-1-carboxylic acid
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Used in the synthesis of pharmaceutical agents, particularly as an intermediate in developing enzyme inhibitors. Its structure supports binding to specific biological targets, making it valuable in drug discovery for metabolic and inflammatory diseases. The compound's stereochemistry enhances selectivity in receptor interactions, improving efficacy and reducing side effects in final drug formulations. It is also employed in research settings to study structure-activity relationships in sulfonamide-based

Used in the synthesis of pharmaceutical agents, particularly as an intermediate in developing enzyme inhibitors. Its structure supports binding to specific biological targets, making it valuable in drug discovery for metabolic and inflammatory diseases. The compound's stereochemistry enhances selectivity in receptor interactions, improving efficacy and reducing side effects in final drug formulations. It is also employed in research settings to study structure-activity relationships in sulfonamide-based therapeutics.

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