(S)-4-(tert-Butoxy)-2-methyl-4-oxobutanoic acid

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Reagent Code: #38502
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CAS Number 182007-75-6

science Other reagents with same CAS 182007-75-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.22 g/mol
Formula C₉H₁₆O₄
badge Registry Numbers
MDL Number MFCD19382513
thermostat Physical Properties
Boiling Point 281.9±23.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.071±0.06 g/cm3(Predicted)
Storage Room temperature, sealed, dry

description Product Description

This chemical is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of chiral compounds. Its structure, featuring a tert-butoxy group and a methyl substituent, makes it a valuable building block for creating complex molecules with specific stereochemistry. It is often employed in the production of active pharmaceutical ingredients (APIs) where precise chiral control is essential. Additionally, it finds application in organic synthesis for constructing ester and carboxylic acid derivatives, which are key components in various drug discovery and development processes. Its stability and reactivity under controlled conditions make it a reliable reagent in medicinal chemistry and fine chemical manufacturing.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,562.00
inventory 250mg
10-20 days ฿2,061.00
inventory 5g
10-20 days ฿19,449.00

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(S)-4-(tert-Butoxy)-2-methyl-4-oxobutanoic acid
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This chemical is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of chiral compounds. Its structure, featuring a tert-butoxy group and a methyl substituent, makes it a valuable building block for creating complex molecules with specific stereochemistry. It is often employed in the production of active pharmaceutical ingredients (APIs) where precise chiral control is essential. Additionally, it finds application in organic synthesis for constructing est

This chemical is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of chiral compounds. Its structure, featuring a tert-butoxy group and a methyl substituent, makes it a valuable building block for creating complex molecules with specific stereochemistry. It is often employed in the production of active pharmaceutical ingredients (APIs) where precise chiral control is essential. Additionally, it finds application in organic synthesis for constructing ester and carboxylic acid derivatives, which are key components in various drug discovery and development processes. Its stability and reactivity under controlled conditions make it a reliable reagent in medicinal chemistry and fine chemical manufacturing.

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