tert-Butyl (1-chloroethyl) carbonate

95%

Reagent Code: #130685
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CAS Number 98015-51-1

science Other reagents with same CAS 98015-51-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.63 g/mol
Formula C₇H₁₃ClO₃
badge Registry Numbers
MDL Number MFCD20621700
thermostat Physical Properties
Boiling Point 58-60 °C at 10 mmHg
inventory_2 Storage & Handling
Density 1.089±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used primarily as a protecting group reagent in organic synthesis, especially in the preparation and modification of peptides and nucleotides. It allows selective protection of amine functionalities due to its stability under various reaction conditions and can be removed under mild acidic conditions. Commonly employed in pharmaceutical synthesis where controlled deprotection is required. Its chloroethyl moiety enables efficient deprotection through solvolysis, making it valuable in multi-step synthetic routes. Also utilized in the development of agrochemicals and specialty polymers requiring precise functional group manipulation.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,280.00
inventory 250mg
10-20 days ฿5,590.00

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tert-Butyl (1-chloroethyl) carbonate
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Used primarily as a protecting group reagent in organic synthesis, especially in the preparation and modification of peptides and nucleotides. It allows selective protection of amine functionalities due to its stability under various reaction conditions and can be removed under mild acidic conditions. Commonly employed in pharmaceutical synthesis where controlled deprotection is required. Its chloroethyl moiety enables efficient deprotection through solvolysis, making it valuable in multi-step synthetic

Used primarily as a protecting group reagent in organic synthesis, especially in the preparation and modification of peptides and nucleotides. It allows selective protection of amine functionalities due to its stability under various reaction conditions and can be removed under mild acidic conditions. Commonly employed in pharmaceutical synthesis where controlled deprotection is required. Its chloroethyl moiety enables efficient deprotection through solvolysis, making it valuable in multi-step synthetic routes. Also utilized in the development of agrochemicals and specialty polymers requiring precise functional group manipulation.

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