(S)-tert-Butyl 3-(pyridin-2-yloxy)pyrrolidine-1-carboxylate

95%

Reagent Code: #38412
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CAS Number 1224514-70-8

science Other reagents with same CAS 1224514-70-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.3202 g/mol
Formula C₁₄H₂₀N₂O₃
badge Registry Numbers
MDL Number MFCD21606420
inventory_2 Storage & Handling
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description Product Description

This chemical is primarily utilized in the pharmaceutical and organic synthesis industries as a key intermediate in the production of biologically active compounds. Its structure, featuring a pyrrolidine ring and a pyridine moiety, makes it valuable for designing and synthesizing molecules with potential therapeutic applications. It is often employed in the development of drugs targeting neurological disorders, inflammation, and other medical conditions due to its ability to interact with specific biological targets. Additionally, its tert-butyloxycarbonyl (Boc) protecting group enhances its stability during synthetic processes, making it a versatile building block in medicinal chemistry.

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inventory 100mg
10-20 days ฿5,508.00

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(S)-tert-Butyl 3-(pyridin-2-yloxy)pyrrolidine-1-carboxylate
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This chemical is primarily utilized in the pharmaceutical and organic synthesis industries as a key intermediate in the production of biologically active compounds. Its structure, featuring a pyrrolidine ring and a pyridine moiety, makes it valuable for designing and synthesizing molecules with potential therapeutic applications. It is often employed in the development of drugs targeting neurological disorders, inflammation, and other medical conditions due to its ability to interact with specific biolog

This chemical is primarily utilized in the pharmaceutical and organic synthesis industries as a key intermediate in the production of biologically active compounds. Its structure, featuring a pyrrolidine ring and a pyridine moiety, makes it valuable for designing and synthesizing molecules with potential therapeutic applications. It is often employed in the development of drugs targeting neurological disorders, inflammation, and other medical conditions due to its ability to interact with specific biological targets. Additionally, its tert-butyloxycarbonyl (Boc) protecting group enhances its stability during synthetic processes, making it a versatile building block in medicinal chemistry.

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