(R)-N-((R)-1-(5-fluoropyridin-2-yl)ethyl)-2-methylpropane-2-sulfinamide

≥95%

Reagent Code: #231935
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CAS Number 1149752-51-1

science Other reagents with same CAS 1149752-51-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.33 g/mol
Formula C₁₁H₁₇FN₂OS
badge Registry Numbers
MDL Number MFCD27957006
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

(R)-N-((R)-1-(5-fluoropyridin-2-yl)ethyl)-2-methylpropane-2-sulfinamide is a chiral intermediate used in pharmaceutical synthesis, particularly for constructing pyridine-containing drug candidates. It acts as a protected derivative of the enantiomerically pure amine (R)-1-(5-fluoropyridin-2-yl)ethanamine, enabling stereocontrolled elaboration in multi-step routes toward bioactive molecules such as kinase inhibitors and CNS-targeted therapies. The tert-butanesulfinamide moiety provides stability during synthetic transformations and can be selectively deprotected to afford the free chiral amine, facilitating efficient production of enantiomerically pure pharmaceuticals.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿54,260.00
(R)-N-((R)-1-(5-fluoropyridin-2-yl)ethyl)-2-methylpropane-2-sulfinamide
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(R)-N-((R)-1-(5-fluoropyridin-2-yl)ethyl)-2-methylpropane-2-sulfinamide is a chiral intermediate used in pharmaceutical synthesis, particularly for constructing pyridine-containing drug candidates. It acts as a protected derivative of the enantiomerically pure amine (R)-1-(5-fluoropyridin-2-yl)ethanamine, enabling stereocontrolled elaboration in multi-step routes toward bioactive molecules such as kinase inhibitors and CNS-targeted therapies. The tert-butanesulfinamide moiety provides stability during sy

(R)-N-((R)-1-(5-fluoropyridin-2-yl)ethyl)-2-methylpropane-2-sulfinamide is a chiral intermediate used in pharmaceutical synthesis, particularly for constructing pyridine-containing drug candidates. It acts as a protected derivative of the enantiomerically pure amine (R)-1-(5-fluoropyridin-2-yl)ethanamine, enabling stereocontrolled elaboration in multi-step routes toward bioactive molecules such as kinase inhibitors and CNS-targeted therapies. The tert-butanesulfinamide moiety provides stability during synthetic transformations and can be selectively deprotected to afford the free chiral amine, facilitating efficient production of enantiomerically pure pharmaceuticals.

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