1,3,5-Triaza-7-phosphaadamantane,min.97% manufacturers
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| | 1,3,5-Triaza-7-phosphaadamantane,min.97% Basic information | | Reaction |
| Product Name: | 1,3,5-Triaza-7-phosphaadamantane,min.97% | | Synonyms: | 1,3,5-Triaza-7-phosphaadamantane,min.97%;1,3,5-TRIAZA-7-PHOSPHAADAMANTANE, MIN. 97%;1,3,5-Triaza-7-phosphatricyclo[3.3.1.13.7]decane, NSC 266642, PTA;1,3,5-Triaza-7-phosphatricyclo[3.3.1.13,7]decane;1,3,5-Triaza-9-phospha-adamantane;Nsc266642;1,3,5-Triaza-7-phosphaadaMantane, Min. 97% PTA;1,3,5-Triaza-7-phosphaadaMantane 97% | | CAS: | 53597-69-6 | | MF: | C6H12N3P | | MW: | 157.15 | | EINECS: | | | Product Categories: | organophosphine ligand | | Mol File: | 53597-69-6.mol |  |
| | 1,3,5-Triaza-7-phosphaadamantane,min.97% Chemical Properties |
| Melting point | 244-250 °C | | Boiling point | 232.5±40.0 °C(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | | pka | 5.78±0.20(Predicted) | | form | Solid | | color | White | | Sensitive | Hygroscopic | | InChI | InChI=1S/C6H12N3P/c1-7-2-9-3-8(1)5-10(4-7)6-9/h1-6H2 | | InChIKey | FXXRPTKTLVHPAR-UHFFFAOYSA-N | | SMILES | N12CN3CP(CN(C3)C1)C2 |
| WGK Germany | 3 | | HS Code | 2934999090 | | Storage Class | 11 - Combustible Solids |
| | 1,3,5-Triaza-7-phosphaadamantane,min.97% Usage And Synthesis |
| Reaction |
- Air-stable, water-soluble version of trimethylphosphine.
- Reagent used in the β-olefination of 2-alkynoates leading to trisubstituted 1,3-dienes.
- Ligand/rhodium catalyst used in the branch selective allylation of acetylacetone.
- Ligand/oxorhenium complex used as a catalyst for the Baeyer-Villiger oxidation of ketones.
| | Uses | - The molecular mechanisms of antimetastatic ruthenium compounds explored through DIGE proteomics.: This study examines the antimetastatic properties of ruthenium compounds using DIGE proteomics. The involvement of 1,3,5-Triaza-7-phosphaadamantane in the complexation with ruthenium and its biological effects were analyzed, highlighting its potential in anticancer therapies (Guidi et al., 2013).
- Synthesis, antimicrobial and antiproliferative activity of novel silver(I) tris(pyrazolyl)methanesulfonate and 1,3,5-triaza-7-phosphadamantane complexes.: This research details the synthesis of novel silver complexes containing 1,3,5-Triaza-7-phosphaadamantane, evaluating their antimicrobial and antiproliferative activities, which demonstrates the compound′s utility in biomedical applications (Pettinari et al., 2011).
| | General Description | Air stable organocatalyst for Baylis-Hillman transformation | | reaction suitability | reagent type: ligand
reaction type: Hydroformylations
reagent type: ligand
reaction type: Hydrogenations
reagent type: ligand
reaction type: Morita-Baylis-Hillman Reactions
reagent type: ligand
reaction type: Sonogashira Coupling
reagent type: ligand
reaction type: Suzuki-Miyaura Coupling |
| | 1,3,5-Triaza-7-phosphaadamantane,min.97% Preparation Products And Raw materials |
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