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Thalidomide-O-C3-Br Size:50mg The two-step reaction procedure involves

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Description

The two-step reaction procedure involves a copper-catalyzed triazole formation of an azide and an alkyne

thus all the instrument settings of the 6-ROX conjugates would be applicable to the applications of 6-ROX alkyne conjugates

08 SMILES [2H]C([2H])([2H])C(=O)NC1=CC=CC(Br)=C1 Purity (HPLC) >= 95% Shipping Conditions Room temperature Storage Conditions Refrigerated Shelf Life 12 months after the date of delivery Regulatory Statement For Research Use Only

Product Name Thalidomide-O-acetamido-PEG6-OH Synonyms Thalidomide-4'-O-acetamido-PEG6-OH CAS Number n/a Related CAS Molecular Formula C25H33N3O11 Molecular Weight 551

Sulforhodamine 101 emits at a longer wavelength than does either Tetramethylrhodamine or Sulforhodamine B

Thalidomide-O-C3-Br Size:50mg The two-step reaction procedure involvesDegrader building block for targeted protein degradation. Contains an E3 ligase ligand with a linker and a function group, which can be conjugated to target protein ligands through straightforward chemical reactions. Product Name Thalidomide O C3 Br Synonyms Thalidomide 4' O C3 Br CAS Number n a Related CAS Molecular Formula C16H15BrN2O5 Molecular Weight 395. 209 SMILES BrCCCOC1=C2C(=O)N(C3CCC(=O)NC3=O)C(=O)C2=CC=C1 Purity (HPLC) >= 95% Shipping

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