Tert-butyl 3-iodoazetidine-1-carboxylate

95%

Reagent Code: #240263
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CAS Number 254454-54-1

science Other reagents with same CAS 254454-54-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 283.10 g/mol
Formula C₈H₁₄INO₂
badge Registry Numbers
MDL Number MFCD09752821
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of biologically active molecules. Its structure allows for selective functionalization at the azetidine ring, making it valuable in medicinal chemistry for constructing constrained ring systems that improve metabolic stability and binding affinity. Commonly employed in cross-coupling reactions due to the presence of the iodine atom, enabling carbon–carbon bond formation. Also utilized in the preparation of protease inhibitors and receptor modulators, where the tert-butyl carbamate (Boc) group provides protection during multi-step syntheses.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿600.00
inventory 25g
10-20 days ฿2,750.00
Tert-butyl 3-iodoazetidine-1-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of biologically active molecules. Its structure allows for selective functionalization at the azetidine ring, making it valuable in medicinal chemistry for constructing constrained ring systems that improve metabolic stability and binding affinity. Commonly employed in cross-coupling reactions due to the presence of the iodine atom, enabling carbon–carbon bond formation. Also utilized in the preparati

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of biologically active molecules. Its structure allows for selective functionalization at the azetidine ring, making it valuable in medicinal chemistry for constructing constrained ring systems that improve metabolic stability and binding affinity. Commonly employed in cross-coupling reactions due to the presence of the iodine atom, enabling carbon–carbon bond formation. Also utilized in the preparation of protease inhibitors and receptor modulators, where the tert-butyl carbamate (Boc) group provides protection during multi-step syntheses.

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