1-Methanesulfonylazetidin-3-amine

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Reagent Code: #214152
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CAS Number 1340300-17-5

science Other reagents with same CAS 1340300-17-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 150.20 g/mol
Formula C₄H₁₀N₂O₂S
badge Registry Numbers
MDL Number MFCD18881108
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of biologically active molecules targeting neurological and inflammatory conditions. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building nitrogen-containing heterocycles. Commonly employed in the preparation of kinase inhibitors and receptor modulators due to its favorable reactivity and stability in multi-step reactions. Also utilized in the design of novel drug candidates requiring constrained amine scaffolds for improved selectivity and metabolic resistance.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿76,620.00
1-Methanesulfonylazetidin-3-amine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of biologically active molecules targeting neurological and inflammatory conditions. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building nitrogen-containing heterocycles. Commonly employed in the preparation of kinase inhibitors and receptor modulators due to its favorable reactivity and stability in multi-step reactions. Also utilized in the design

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of biologically active molecules targeting neurological and inflammatory conditions. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building nitrogen-containing heterocycles. Commonly employed in the preparation of kinase inhibitors and receptor modulators due to its favorable reactivity and stability in multi-step reactions. Also utilized in the design of novel drug candidates requiring constrained amine scaffolds for improved selectivity and metabolic resistance.

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