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About This Item
form
beads
Quality Level
composition
loading, 4-6 wt. %
5 wt% loading
reaction suitability
reagent type: catalyst
core: palladium
reaction type: Cross Couplings
color
white to beige-brown
SMILES string
[Na+].Nc1ccccc1-c2ccccc2[Pd]Cl.COc3ccc(c(OC)c3-c4ccccc4P(C5CCCCC5)C6CCCCC6)S([O-])(=O)=O
InChI
1S/C26H35O5PS.C12H10N.ClH.Na.Pd/c1-30-22-17-18-24(33(27,28)29)26(31-2)25(22)21-15-9-10-16-23(21)32(19-11-5-3-6-12-19)20-13-7-4-8-14-20;13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;;;/h9-10,15-20H,3-8,11-14H2,1-2H3,(H,27,28,29);1-6,8-9H,13H2;1H;;/q;;;2*+1/p-2
InChI key
MWQYWXJKMDRSJN-UHFFFAOYSA-L
General description
- DNA-compatible Suzuki-Miyaura reaction between DNA-linked aryl halides and various boronic acids/esters including heteroaryl boronates.
- DNA-compatible hydroxycarbonylation reactions.
- The cross-coupling reaction between boronic ester and brominated cyclic nucleotide to synthesize cyclic adenosine and guanosine monophosphate in the presence of potassium phosphate and hydrochloric acid.
- The Palladium-Mediated Carbonylative Suzuki Coupling for DNA-Encoded Library Synthesis
- In Multiplexed CuAAC Suzuki–Miyaura Labeling for Tandem Activity-Based Chemoproteomic Profiling
Application
For general uses, product is also available in powdered form (763314 )
Features and Benefits
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