1-(9H-Fluoren-9-yl)-3-oxo-2,7,10,13,16-pentaoxa-4-azanonadecan-19-oic acid
98%
Reagent
Code: #119726
CAS Number
557756-85-1
blur_circular Chemical Specifications
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Molecular Information
Weight
487.54 g/mol
Formula
C₂₆H₃₃NO₈
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Registry Numbers
MDL Number
MFCD06656472
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Storage & Handling
Storage
2-8°C, dry and sealed
description Product Description
This compound is primarily utilized in the field of bioconjugation and peptide synthesis. It serves as a versatile linker molecule, enabling the attachment of various functional groups or biomolecules to solid supports or other molecules. Its structure, featuring a fluorenyl group and multiple ether linkages, makes it particularly useful for creating stable, yet cleavable, connections in complex chemical assemblies. This is especially valuable in the development of targeted drug delivery systems, where precise control over the release of active compounds is crucial. Additionally, it finds application in the synthesis of peptide-based therapeutics, where it aids in the efficient and selective modification of peptide chains, enhancing their stability and bioavailability.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | Colorless to yellow liquid |
Purity (%) | 97.5-100% |
Infrared Spectrum | Conforms To Structure |
NMR | Conforms To Structure |
shopping_cart Available Sizes & Pricing
1-(9H-Fluoren-9-yl)-3-oxo-2,7,10,13,16-pentaoxa-4-azanonadecan-19-oic acid
This compound is primarily utilized in the field of bioconjugation and peptide synthesis. It serves as a versatile linker molecule, enabling the attachment of various functional groups or biomolecules to solid supports or other molecules. Its structure, featuring a fluorenyl group and multiple ether linkages, makes it particularly useful for creating stable, yet cleavable, connections in complex chemical assemblies. This is especially valuable in the development of targeted drug delivery systems, where precise control over the release of active compounds is crucial. Additionally, it finds application in the synthesis of peptide-based therapeutics, where it aids in the efficient and selective modification of peptide chains, enhancing their stability and bioavailability.
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