(-)-tert-Butyl (S)-2-hydroxybutyrate

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Reagent Code: #38342
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CAS Number 37787-90-9

science Other reagents with same CAS 37787-90-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 160.21 g/mol
Formula C₈H₁₆O₃
thermostat Physical Properties
Melting Point 50-54℃(lit.)
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) that require specific stereochemistry. It serves as an intermediate in the preparation of compounds with potential therapeutic applications, such as antiviral or anticancer agents. Additionally, it is employed in organic synthesis to introduce the tert-butyl ester group, which can act as a protecting group for carboxylic acids during complex chemical reactions. Its (S)-configuration makes it valuable in asymmetric synthesis, where enantioselectivity is crucial for achieving desired biological activity.

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inventory 50mg
10-20 days ฿7,119.00

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(-)-tert-Butyl (S)-2-hydroxybutyrate
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) that require specific stereochemistry. It serves as an intermediate in the preparation of compounds with potential therapeutic applications, such as antiviral or anticancer agents. Additionally, it is employed in organic synthesis to introduce the tert-butyl ester group, which can act as a protecting group for carboxylic acids during complex chemical reactions. I

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) that require specific stereochemistry. It serves as an intermediate in the preparation of compounds with potential therapeutic applications, such as antiviral or anticancer agents. Additionally, it is employed in organic synthesis to introduce the tert-butyl ester group, which can act as a protecting group for carboxylic acids during complex chemical reactions. Its (S)-configuration makes it valuable in asymmetric synthesis, where enantioselectivity is crucial for achieving desired biological activity.

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