(S)-(2,2-Dimethyl-1,3-Dioxolan-4-Yl)Methyl 3-(4-Hydroxyphenyl)Propanoate

99%

Reagent Code: #237511
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CAS Number 144256-11-1

science Other reagents with same CAS 144256-11-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 280.32 g/mol
Formula C₁₅H₂₀O₅
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly chiral compounds featuring a protected diol moiety and a 3-(4-hydroxyphenyl)propanoate structure. This enables the creation of bioactive molecules with high stereoselectivity, valuable for active pharmaceutical ingredients (APIs) in anti-inflammatory, antioxidant, cardiovascular, and metabolic therapies. Commonly employed in research to construct complex organic molecules where stereochemistry and controlled release properties are essential for biological activity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿680.00
inventory 1g
10-20 days ฿1,850.00
inventory 5g
10-20 days ฿6,110.00
inventory 25g
10-20 days ฿20,020.00
(S)-(2,2-Dimethyl-1,3-Dioxolan-4-Yl)Methyl 3-(4-Hydroxyphenyl)Propanoate
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Used in the synthesis of pharmaceutical intermediates, particularly chiral compounds featuring a protected diol moiety and a 3-(4-hydroxyphenyl)propanoate structure. This enables the creation of bioactive molecules with high stereoselectivity, valuable for active pharmaceutical ingredients (APIs) in anti-inflammatory, antioxidant, cardiovascular, and metabolic therapies. Commonly employed in research to construct complex organic molecules where stereochemistry and controlled release properties are essent

Used in the synthesis of pharmaceutical intermediates, particularly chiral compounds featuring a protected diol moiety and a 3-(4-hydroxyphenyl)propanoate structure. This enables the creation of bioactive molecules with high stereoselectivity, valuable for active pharmaceutical ingredients (APIs) in anti-inflammatory, antioxidant, cardiovascular, and metabolic therapies. Commonly employed in research to construct complex organic molecules where stereochemistry and controlled release properties are essential for biological activity.

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