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CAS Number: 446822-71-5
Empirical Formula (Hill Notation): C15H18BOPS
Molecular Weight: 288.15
| Related Categories | Catalysis and Inorganic Chemistry, Chemical Biology, Chemical Ligation, Chemical Synthesis, Other Ligands, |
| assay | ≥98.0% |
| mp | 52-55 °C |
| storage temp. | 2-8°C |
1 g in glass btl
250 mg in glass btl
Sold under license for research and development purposes only. US Patent 6,974,884 and related patents apply
Customers Also Viewed
| Symbol | GHS07 |
| Signal word | Warning |
| Hazard statements | H315-H319-H335 |
| Precautionary statements | P261-P305 + P351 + P338 |
| Personal Protective Equipment | dust mask type N95 (US), Eyeshields, Gloves |
| WGK Germany | 3 |
Chemoselective ligation strategies are a key success factor for chemical biology research. Ligation techniques open pathways to fully synthetic large peptides and even proteins. They have proven to b...
Chemfiles Volume 10 Article 2
Keywords: 1,3-Dipolar cycloaddition, Acetylations, Building blocks, Catalog, Catalysis, Chemical biology, Cyclizations, Cycloadditions, Eliminations, Immobilization, Metal organic frameworks, Molecular probes, Nanotubes, Oxidations, Peptide synthesis, Pharmaceutical, Purification, Reductions, Staudinger Reaction
The reaction between an azide and a phosphine forming an aza-ylide was discovered almost a century ago by Nobel Prize laureate Herrmann Staudinger. It has found widespread application in chemical syn...
Matthias Junkers
Aldrich ChemFiles 2008, 8.1, 7.
Keywords: Amidations, Catalysis, Cyclizations, Eliminations, Esterifications, Glycosylations, Iodinations, Molecular probes, PAGE, Peptide synthesis, Reductions, Solid phase peptide synthesis, Staudinger Reaction, Staudinger Reduction, Wittig Reaction
Although the previously described methods for Staudinger ligations work well even in biological environments, a modification forming a native amide bond without leaving the unnatural phosphine oxide ...
Matthias Junkers
Aldrich ChemFiles 2008, 8.1, 9.
Keywords: Catalysis, PAGE, Peptide synthesis, Solid phase peptide synthesis
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