tert-Butyl 6-Chloro-5(S)-hydroxy-3-oxohexanoate

98%

Reagent Code: #51420
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CAS Number 154026-92-3

science Other reagents with same CAS 154026-92-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.69 g/mol
Formula C₁₀H₁₇ClO₄
badge Registry Numbers
MDL Number MFCD02093052
inventory_2 Storage & Handling
Storage −20°C, inert gas

description Product Description

This chemical is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various active pharmaceutical ingredients (APIs). Its structure, featuring both hydroxyl and ester functional groups, makes it a versatile building block for creating chiral compounds, which are crucial in the development of enantiomerically pure drugs. Additionally, it is employed in the preparation of intermediates for cholesterol-lowering agents and other therapeutic compounds. Its role in asymmetric synthesis highlights its importance in producing high-purity, biologically active molecules.

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Test Parameter Specification
Appearance Pale Yellow to Pale Brown Oil
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿14,463.00

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tert-Butyl 6-Chloro-5(S)-hydroxy-3-oxohexanoate
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This chemical is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various active pharmaceutical ingredients (APIs). Its structure, featuring both hydroxyl and ester functional groups, makes it a versatile building block for creating chiral compounds, which are crucial in the development of enantiomerically pure drugs. Additionally, it is employed in the preparation of intermediates for chole

This chemical is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various active pharmaceutical ingredients (APIs). Its structure, featuring both hydroxyl and ester functional groups, makes it a versatile building block for creating chiral compounds, which are crucial in the development of enantiomerically pure drugs. Additionally, it is employed in the preparation of intermediates for cholesterol-lowering agents and other therapeutic compounds. Its role in asymmetric synthesis highlights its importance in producing high-purity, biologically active molecules.

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