(S)-2-Acetamido-4-(tert-butoxy)-4-oxobutanoic acid

98%

Reagent Code: #234984
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CAS Number 117833-18-8

science Other reagents with same CAS 117833-18-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.25 g/mol
Formula C₁₀H₁₇NO₅
badge Registry Numbers
MDL Number MFCD00236746
thermostat Physical Properties
Boiling Point 449.6°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected carboxylic acid and amide functionalities make it suitable for peptide-like structures, enabling selective transformations in multi-step organic syntheses. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its stereochemical purity and functional group compatibility.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿154.00
inventory 1g
10-20 days ฿198.00
inventory 5g
10-20 days ฿1,470.00
inventory 25g
10-20 days ฿4,360.00
(S)-2-Acetamido-4-(tert-butoxy)-4-oxobutanoic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected carboxylic acid and amide functionalities make it suitable for peptide-like structures, enabling selective transformations in multi-step organic syntheses. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its stereochemical purity and functional group compatibility.

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected carboxylic acid and amide functionalities make it suitable for peptide-like structures, enabling selective transformations in multi-step organic syntheses. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its stereochemical purity and functional group compatibility.

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