1,3-Dioxoisoindolin-2-yl 4-phenylbutanoate

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Reagent Code: #179568
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CAS Number 1841512-58-0

science Other reagents with same CAS 1841512-58-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 309.321 g/mol
Formula C₁₈H₁₅NO₄
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

1,3-Dioxoisoindolin-2-yl 4-phenylbutanoate is a specialty organic intermediate used in fine chemical and pharmaceutical synthesis. The phthalimide (1,3-dioxoisoindolin-2-yl) group serves as a protecting moiety for hydroxylamine derivatives, facilitating selective reactions in multi-step syntheses. The 4-phenylbutanoate chain imparts hydrophobic character, making it suitable for constructing molecules with potential biological activity, such as analgesics or anti-inflammatory agents. It is employed in ester-based coupling reactions and as a building block for complex APIs, offering stability and compatibility in polar aprotic solvents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,590.00
inventory 1g
10-20 days ฿4,270.00
inventory 5g
10-20 days ฿17,400.00

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1,3-Dioxoisoindolin-2-yl 4-phenylbutanoate
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1,3-Dioxoisoindolin-2-yl 4-phenylbutanoate is a specialty organic intermediate used in fine chemical and pharmaceutical synthesis. The phthalimide (1,3-dioxoisoindolin-2-yl) group serves as a protecting moiety for hydroxylamine derivatives, facilitating selective reactions in multi-step syntheses. The 4-phenylbutanoate chain imparts hydrophobic character, making it suitable for constructing molecules with potential biological activity, such as analgesics or anti-inflammatory agents. It is employed in est

1,3-Dioxoisoindolin-2-yl 4-phenylbutanoate is a specialty organic intermediate used in fine chemical and pharmaceutical synthesis. The phthalimide (1,3-dioxoisoindolin-2-yl) group serves as a protecting moiety for hydroxylamine derivatives, facilitating selective reactions in multi-step syntheses. The 4-phenylbutanoate chain imparts hydrophobic character, making it suitable for constructing molecules with potential biological activity, such as analgesics or anti-inflammatory agents. It is employed in ester-based coupling reactions and as a building block for complex APIs, offering stability and compatibility in polar aprotic solvents.

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