4-[1-[(2-Methylpropan-2-yl)oxycarbonyl]azetidin-3-yl]oxybenzoicacid

95%

Reagent Code: #213629
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CAS Number 1259323-78-8

science Other reagents with same CAS 1259323-78-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 293.32 g/mol
Formula C₁₅H₁₉NO₅
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MDL Number MFCD18089675
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of beta-lactam antibiotics. Its structure supports the construction of complex molecules by providing a protected azetidine ring, which is key in creating biologically active compounds. The tert-butyloxycarbonyl (Boc) group allows for selective protection of nitrogen, enabling controlled reactions in multi-step syntheses. The benzoic acid moiety can be further modified to link with other pharmacophores, making it valuable in medicinal chemistry for designing drug candidates with improved stability and binding properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,890.00
inventory 250mg
10-20 days ฿6,490.00
inventory 5g
10-20 days ฿43,680.00
inventory 1g
10-20 days ฿12,900.00
4-[1-[(2-Methylpropan-2-yl)oxycarbonyl]azetidin-3-yl]oxybenzoicacid
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of beta-lactam antibiotics. Its structure supports the construction of complex molecules by providing a protected azetidine ring, which is key in creating biologically active compounds. The tert-butyloxycarbonyl (Boc) group allows for selective protection of nitrogen, enabling controlled reactions in multi-step syntheses. The benzoic acid moiety can be further modified to link with other pharmacophores, making it valuabl

Used as an intermediate in pharmaceutical synthesis, particularly in the development of beta-lactam antibiotics. Its structure supports the construction of complex molecules by providing a protected azetidine ring, which is key in creating biologically active compounds. The tert-butyloxycarbonyl (Boc) group allows for selective protection of nitrogen, enabling controlled reactions in multi-step syntheses. The benzoic acid moiety can be further modified to link with other pharmacophores, making it valuable in medicinal chemistry for designing drug candidates with improved stability and binding properties.

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