1-(Cyclooct-4-en-1-yloxy)-1-oxo-5,8,11-trioxa-2-azatetradecan-14-oic acid

95%

Reagent Code: #157025
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CAS Number 2141981-86-2

science Other reagents with same CAS 2141981-86-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 373.44 g/mol
Formula C₁₈H₃₁NO₇
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MDL Number MFCD31811538
inventory_2 Storage & Handling
Storage -20°C, light-proof, inert gas

description Product Description

Used in advanced polymer synthesis as a functional linker due to its long hydrophilic chain and reactive carboxylic acid end group. Its structure allows incorporation into amphiphilic copolymers for drug delivery systems, particularly in forming micelles that encapsulate hydrophobic drugs. The cyclooctenyl group enables click chemistry applications via ring-opening metathesis or photochemical reactions, making it valuable in bioconjugation and surface modification. Also employed in creating biodegradable hydrogels for tissue engineering, where the ether-oxygen rich segment enhances flexibility and water retention.

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inventory 100mg
10-20 days ฿105,000.00

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1-(Cyclooct-4-en-1-yloxy)-1-oxo-5,8,11-trioxa-2-azatetradecan-14-oic acid
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Used in advanced polymer synthesis as a functional linker due to its long hydrophilic chain and reactive carboxylic acid end group. Its structure allows incorporation into amphiphilic copolymers for drug delivery systems, particularly in forming micelles that encapsulate hydrophobic drugs. The cyclooctenyl group enables click chemistry applications via ring-opening metathesis or photochemical reactions, making it valuable in bioconjugation and surface modification. Also employed in creating biodegradable

Used in advanced polymer synthesis as a functional linker due to its long hydrophilic chain and reactive carboxylic acid end group. Its structure allows incorporation into amphiphilic copolymers for drug delivery systems, particularly in forming micelles that encapsulate hydrophobic drugs. The cyclooctenyl group enables click chemistry applications via ring-opening metathesis or photochemical reactions, making it valuable in bioconjugation and surface modification. Also employed in creating biodegradable hydrogels for tissue engineering, where the ether-oxygen rich segment enhances flexibility and water retention.

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