1-(((4-Nitrophenoxy)carbonyl)oxy)ethyl isobutyrate

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Reagent Code: #39063
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CAS Number 194995-47-6

science Other reagents with same CAS 194995-47-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.2607 g/mol
Formula C₁₃H₁₅NO₇
badge Registry Numbers
MDL Number MFCD22571566
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is a specialty chemical intermediate primarily used in pharmaceutical synthesis for prodrug development. It is the 4-nitrophenyl carbonate ester of 1-hydroxyethyl isobutyrate, acting as an activated electrophile. It reacts readily with primary and secondary amines to form 1-(isobutyryloxy)ethyl carbamate prodrugs, which provide controlled enzymatic release of the parent amine API, improving solubility, bioavailability, and pharmacokinetics.

Additionally, it finds applications in advanced organic synthesis requiring selective carbonate formation or functional group protection.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,743.00

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1-(((4-Nitrophenoxy)carbonyl)oxy)ethyl isobutyrate
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This compound is a specialty chemical intermediate primarily used in pharmaceutical synthesis for prodrug development. It is the 4-nitrophenyl carbonate ester of 1-hydroxyethyl isobutyrate, acting as an activated electrophile. It reacts readily with primary and secondary amines to form 1-(isobutyryloxy)ethyl carbamate prodrugs, which provide controlled enzymatic release of the parent amine API, improving solubility, bioavailability, and pharmacokinetics.

Additionally, it finds applications in advan

This compound is a specialty chemical intermediate primarily used in pharmaceutical synthesis for prodrug development. It is the 4-nitrophenyl carbonate ester of 1-hydroxyethyl isobutyrate, acting as an activated electrophile. It reacts readily with primary and secondary amines to form 1-(isobutyryloxy)ethyl carbamate prodrugs, which provide controlled enzymatic release of the parent amine API, improving solubility, bioavailability, and pharmacokinetics.

Additionally, it finds applications in advanced organic synthesis requiring selective carbonate formation or functional group protection.

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