2-1-[(tert-butoxy)carbonyl]azetidin-3-ylbenzoicacid

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Reagent Code: #244338
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CAS Number 908334-12-3

science Other reagents with same CAS 908334-12-3

blur_circular Chemical Specifications

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Weight 277.32 g/mol
Formula C₁₅H₁₉NO₄
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Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of beta-lactam antibiotics. Its structure supports the construction of complex molecules by providing a protected azetidine ring, which is valuable in medicinal chemistry for enhancing metabolic stability and bioavailability. Commonly employed in solid-phase and solution-phase peptide-like synthesis where selective protection and mild deprotection are required. Also utilized in research settings for creating enzyme inhibitors and receptor ligands due to its conformational rigidity and functional group compatibility.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿19,340.00
inventory 50mg
10-20 days ฿27,180.00
inventory 100mg
10-20 days ฿40,500.00
inventory 250mg
10-20 days ฿57,710.00
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2-1-[(tert-butoxy)carbonyl]azetidin-3-ylbenzoicacid
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of beta-lactam antibiotics. Its structure supports the construction of complex molecules by providing a protected azetidine ring, which is valuable in medicinal chemistry for enhancing metabolic stability and bioavailability. Commonly employed in solid-phase and solution-phase peptide-like synthesis where selective protection and mild deprotection are required. Also utilized in research settings for crea

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of beta-lactam antibiotics. Its structure supports the construction of complex molecules by providing a protected azetidine ring, which is valuable in medicinal chemistry for enhancing metabolic stability and bioavailability. Commonly employed in solid-phase and solution-phase peptide-like synthesis where selective protection and mild deprotection are required. Also utilized in research settings for creating enzyme inhibitors and receptor ligands due to its conformational rigidity and functional group compatibility.

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