TERT-BUTYL N-(2-OXIRANYLMETHYL)CARBAMATE

95%

Reagent Code: #240473
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CAS Number 115198-80-6

science Other reagents with same CAS 115198-80-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.21 g/mol
Formula C₈H₁₅NO₃
badge Registry Numbers
MDL Number MFCD05664375
thermostat Physical Properties
Melting Point 48 °C
Boiling Point 262.9±13.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.041 g/mL at 25 °C(lit.)
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of active pharmaceutical ingredients, particularly in the development of protease inhibitors and other bioactive molecules. Its epoxide functionality allows for selective ring-opening reactions, enabling the introduction of complex side chains in drug structures. Commonly employed in medicinal chemistry for building chiral intermediates due to its reactivity and stability under various reaction conditions. Also utilized in the preparation of specialty polymers and functionalized resins where controlled cross-linking or grafting is required.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,650.00

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TERT-BUTYL N-(2-OXIRANYLMETHYL)CARBAMATE
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Used as a key intermediate in the synthesis of active pharmaceutical ingredients, particularly in the development of protease inhibitors and other bioactive molecules. Its epoxide functionality allows for selective ring-opening reactions, enabling the introduction of complex side chains in drug structures. Commonly employed in medicinal chemistry for building chiral intermediates due to its reactivity and stability under various reaction conditions. Also utilized in the preparation of specialty polymers

Used as a key intermediate in the synthesis of active pharmaceutical ingredients, particularly in the development of protease inhibitors and other bioactive molecules. Its epoxide functionality allows for selective ring-opening reactions, enabling the introduction of complex side chains in drug structures. Commonly employed in medicinal chemistry for building chiral intermediates due to its reactivity and stability under various reaction conditions. Also utilized in the preparation of specialty polymers and functionalized resins where controlled cross-linking or grafting is required.

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