(E)-Cyclooct-4-en-1-yl (2,5-dioxopyrrolidin-1-yl) carbonate

≥83%

Reagent Code: #181032
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CAS Number 1191901-33-3

science Other reagents with same CAS 1191901-33-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 267.28 g/mol
Formula C₁₃H₁₇NO₅
badge Registry Numbers
MDL Number MFCD24386372
inventory_2 Storage & Handling
Storage -20°C, stored in inert gas, avoiding light

description Product Description

Used as an activated carbonate reagent in organic synthesis for the efficient formation of carbamates by reacting with amines. The N-hydroxysuccinimide (NHS) group facilitates selective coupling under mild conditions, making it valuable in peptide synthesis, bioconjugate preparation, and the introduction of linker groups. The (E)-cyclooctenyl moiety acts as a traceless or cleavable linker in solid-phase synthesis or targeted delivery systems, owing to the alkene functionality that enables further modifications such as olefin metathesis or hydrogenation. Its stability across various solvents and controlled reactivity support its application in multi-step sequences with orthogonal protection strategies.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿2,560.00
inventory 25mg
10-20 days ฿18,720.00
inventory 5mg
10-20 days ฿7,280.00

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(E)-Cyclooct-4-en-1-yl (2,5-dioxopyrrolidin-1-yl) carbonate
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Used as an activated carbonate reagent in organic synthesis for the efficient formation of carbamates by reacting with amines. The N-hydroxysuccinimide (NHS) group facilitates selective coupling under mild conditions, making it valuable in peptide synthesis, bioconjugate preparation, and the introduction of linker groups. The (E)-cyclooctenyl moiety acts as a traceless or cleavable linker in solid-phase synthesis or targeted delivery systems, owing to the alkene functionality that enables further modific

Used as an activated carbonate reagent in organic synthesis for the efficient formation of carbamates by reacting with amines. The N-hydroxysuccinimide (NHS) group facilitates selective coupling under mild conditions, making it valuable in peptide synthesis, bioconjugate preparation, and the introduction of linker groups. The (E)-cyclooctenyl moiety acts as a traceless or cleavable linker in solid-phase synthesis or targeted delivery systems, owing to the alkene functionality that enables further modifications such as olefin metathesis or hydrogenation. Its stability across various solvents and controlled reactivity support its application in multi-step sequences with orthogonal protection strategies.

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