Molecular structure of 2-Tributylstannylthiazole, CAS Number: 121359-48-6
2-Tributylstannylthiazole (CAS 121359-48-6)
CAS Number:
121359-48-6
Molecular Weight:
374.17
Molecular Formula:
C15H29NSSn
Supplemental Information:
This is as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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2-Tributylstannylthiazole (2-TBT) is a well-studied organostannane compound with significant potential in organic synthesis, and scientific research. This versatile compound possesses diverse properties, making it highly appealing for a broad spectrum of applications. Scientific research has extensively employed 2-Tributylstannylthiazole in numerous capacities. It serves as a catalyst for synthesizing various organic compounds and acts as a reagent for producing polymers and other materials. A noteworthy characteristic of 2-Tributylstannylthiazole is its ability to act as a reducing agent. It effectively reduces the oxidation state of other molecules, facilitated by the presence of an acid. This reaction leads to the formation of a tributylstannylthiazole derivative.
2-Tributylstannylthiazole (CAS 121359-48-6) References
- Design, synthesis, and biological evaluation of novel 7-azaindolyl-heteroaryl-maleimides as potent and selective glycogen synthase kinase-3beta (GSK-3beta) inhibitors. | O'Neill, DJ., et al. 2004. Bioorg Med Chem. 12: 3167-85. PMID: 15158785
- Synthesis, structure-activity relationship, and receptor pharmacology of a new series of quinoline derivatives acting as selective, noncompetitive mGlu1 antagonists. | Mabire, D., et al. 2005. J Med Chem. 48: 2134-53. PMID: 15771457
- An efficient unnatural base pair for a base-pair-expanded transcription system. | Mitsui, T., et al. 2005. J Am Chem Soc. 127: 8652-8. PMID: 15954770
- Design of potent, orally available antagonists of the transient receptor potential vanilloid 1. Structure-activity relationships of 2-piperazin-1-yl-1H-benzimidazoles. | Ognyanov, VI., et al. 2006. J Med Chem. 49: 3719-42. PMID: 16759115
- SAR study of bicyclo[4.1.0]heptanes as melanin-concentrating hormone receptor R1 antagonists: taming hERG. | Su, J., et al. 2007. Bioorg Med Chem. 15: 5369-85. PMID: 17572094
- Design and synthesis of human immunodeficiency virus entry inhibitors: sulfonamide as an isostere for the alpha-ketoamide group. | Lu, RJ., et al. 2007. J Med Chem. 50: 6535-44. PMID: 18052117
- Identification of CKD-516: a potent tubulin polymerization inhibitor with marked antitumor activity against murine and human solid tumors. | Lee, J., et al. 2010. J Med Chem. 53: 6337-54. PMID: 20690624
- Phorboxazole Synthetic Studies: Design, Synthesis and Biological Evaluation of Phorboxazole A and Hemi-Phorboxazole A Related Analogues. | Smith, AB., et al. 2011. Tetrahedron. 67: 5069-5078. PMID: 21811346
- Enhancement of cyclization quantum yields of perfluorodiarylethenes via weak intramolecular interactions. | Pu, S., et al. 2013. Chem Commun (Camb). 49: 8036-8. PMID: 23903904
- Negishi cross-coupling enabled synthesis of novel NAD(+)-dependent DNA ligase inhibitors and SAR development. | Murphy-Benenato, KE., et al. 2015. Bioorg Med Chem Lett. 25: 5172-7. PMID: 26463129
- Discovery of Indazole Derivatives as a Novel Class of Bacterial Gyrase B Inhibitors. | Zhang, J., et al. 2015. ACS Med Chem Lett. 6: 1080-5. PMID: 26487916
- Novel Human Neutral Sphingomyelinase 2 Inhibitors as Potential Therapeutics for Alzheimer's Disease. | Šála, M., et al. 2020. J Med Chem. 63: 6028-6056. PMID: 32298582
- Discovery of 4,6- and 5,7-Disubstituted Isoquinoline Derivatives as a Novel Class of Protein Kinase C ζ Inhibitors with Fragment-Merging Strategy. | Atobe, M., et al. 2020. J Med Chem. 63: 7143-7162. PMID: 32551607
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2-Tributylstannylthiazole, 1 g | sc-251803 | 1 g | $142.00 |