Phenyl 1-Chloroethyl Carbonate

95%

Reagent Code: #226443
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CAS Number 50972-20-8

science Other reagents with same CAS 50972-20-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.61896 g/mol
Formula C₉H₉ClO₃
badge Registry Numbers
MDL Number MFCD30719991
thermostat Physical Properties
Boiling Point 67-68 °C
inventory_2 Storage & Handling
Density 1.240±0.06 g/cm3
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of carbamates and esters through alcohol protection and deprotection steps. It serves as a chloroethyl-protecting group for hydroxyl functionalities in complex molecule assembly, such as in pharmaceuticals and natural products. The compound enables selective reactions by temporarily blocking reactive alcohol sites, and the protecting group can be removed under mild basic or acidic conditions. Its reactivity makes it valuable in multi-step syntheses where controlled functional group manipulation is required.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿7,200.00
250mg
10-20 days ฿13,600.00
1g
10-20 days ฿40,000.00
Phenyl 1-Chloroethyl Carbonate
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Used as an intermediate in organic synthesis, particularly in the preparation of carbamates and esters through alcohol protection and deprotection steps. It serves as a chloroethyl-protecting group for hydroxyl functionalities in complex molecule assembly, such as in pharmaceuticals and natural products. The compound enables selective reactions by temporarily blocking reactive alcohol sites, and the protecting group can be removed under mild basic or acidic conditions. Its reactivity makes it valuable in

Used as an intermediate in organic synthesis, particularly in the preparation of carbamates and esters through alcohol protection and deprotection steps. It serves as a chloroethyl-protecting group for hydroxyl functionalities in complex molecule assembly, such as in pharmaceuticals and natural products. The compound enables selective reactions by temporarily blocking reactive alcohol sites, and the protecting group can be removed under mild basic or acidic conditions. Its reactivity makes it valuable in multi-step syntheses where controlled functional group manipulation is required.

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