761516
Dibenzocyclooctyne-acid
95%, storage temp.:-20°C
Sinônimo(s):
DBCO-Acid
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About This Item
Fórmula empírica (Notação de Hill):
C21H19NO3
Peso molecular:
333.38
Número MDL:
Código UNSPSC:
12352106
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Ensaio
95%
Formulário
solid
adequação da reação
reaction type: click chemistry
reagent type: linker
pf
118-125 °C
grupo funcional
carboxylic acid
temperatura de armazenamento
−20°C
cadeia de caracteres SMILES
O=C(CCCCC(O)=O)N1CC2=C(C=CC=C2)C#CC3=C1C=CC=C3
InChI
1S/C21H19NO3/c23-20(11-5-6-12-21(24)25)22-15-18-9-2-1-7-16(18)13-14-17-8-3-4-10-19(17)22/h1-4,7-10H,5-6,11-12,15H2,(H,24,25)
chave InChI
NIRLBCOFKPVQLM-UHFFFAOYSA-N
Descrição geral
Acid functionalized cyclooctyne derivative. Cyclooctynes are useful in strain-promoted copper-free azide-alkyne click chemistry reactions. This azadibenzocyclooctyne will react with azide functionalized compounds or biomolecules without the need for a Cu(I) catalyst to result in a stable triazole linkage.
Aplicação
Dibenzocyclooctyne-acid may be used for the surface modification of eight-arm poly(ethylene glycol), to make it susceptible to strain promoted alkyne-azide cycloaddition (SPAAC) with PEG-bis-azide leading to the formation of hydrogels. These hydrogels are useful for protein immobilization.
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
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