Cholesteryl chloroformate

95%

Reagent Code: #157369
label
Alias Cholesterol chloroformate; Cholesterol chloroformate, Cholesterol-5-ene-3-ol (3β) chloroformate, Cholesterol-formyl chloride, Cholesterol chloroformate
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CAS Number 7144-08-3

science Other reagents with same CAS 7144-08-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 449.11 g/mol
Formula C₂₈H₄₅ClO₂
badge Registry Numbers
EC Number 230-447-9
MDL Number MFCD00003633
thermostat Physical Properties
Melting Point 115-117 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used as a derivatizing agent in organic synthesis, particularly in the preparation of steroidal carbonates and in modifying hydroxyl groups in complex molecules via carbonate formation. It is also employed in the synthesis of liquid crystals and cholesterol-based compounds for research in membrane biology. Its reactivity with alcohols and phenols makes it useful for protecting group strategies, structural analysis in steroid chemistry, and sample preparation for spectroscopic techniques such as NMR or MS to enhance detection sensitivity.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,450.00
inventory 25g
10-20 days ฿5,440.00

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Cholesteryl chloroformate
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Used as a derivatizing agent in organic synthesis, particularly in the preparation of steroidal carbonates and in modifying hydroxyl groups in complex molecules via carbonate formation. It is also employed in the synthesis of liquid crystals and cholesterol-based compounds for research in membrane biology. Its reactivity with alcohols and phenols makes it useful for protecting group strategies, structural analysis in steroid chemistry, and sample preparation for spectroscopic techniques such as NMR or MS to
Used as a derivatizing agent in organic synthesis, particularly in the preparation of steroidal carbonates and in modifying hydroxyl groups in complex molecules via carbonate formation. It is also employed in the synthesis of liquid crystals and cholesterol-based compounds for research in membrane biology. Its reactivity with alcohols and phenols makes it useful for protecting group strategies, structural analysis in steroid chemistry, and sample preparation for spectroscopic techniques such as NMR or MS to enhance detection sensitivity.
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