| Identification | Back Directory | [Name]
1,3,5-Triaza-7-phosphaadamantane,min.97% | [CAS]
53597-69-6 | [Synonyms]
Nsc266642
1,3,5-Triaza-7-phosphaadamantane
1,3,5-Triaza-9-phospha-adamantane
1,3,5-Triaza-7-phosphaadaMantane 97%
1,3,5-Triaza-7-phosphaadamantane,min.97%
1,3,5-TRIAZA-7-PHOSPHAADAMANTANE, MIN. 97%
1,3,5-Triaza-7-phosphaadaMantane, Min. 97% PTA
1,3,5-Triaza-7-phosphatricyclo[3.3.1.13,7]decane
1,3,5-Triaza-7-phosphatricyclo[3.3.1.13.7]decane, NSC 266642, PTA | [Molecular Formula]
C6H12N3P | [MDL Number]
MFCD00154905 | [MOL File]
53597-69-6.mol | [Molecular Weight]
157.15 |
| Chemical Properties | Back Directory | [Melting point ]
244-250 °C | [Boiling point ]
232.5±40.0 °C(Predicted) | [storage temp. ]
Inert atmosphere,2-8°C | [form ]
Solid | [pka]
5.78±0.20(Predicted) | [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 |
| Questions And Answer | Back Directory | [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.
|
| Hazard Information | Back Directory | [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 |
|
| Company Name: |
Energy Chemical
|
| Tel: |
021-021-58432009 400-005-6266 |
| Website: |
http://www.energy-chemical.com |
| Company Name: |
Sigma-Aldrich
|
| Tel: |
021-61415566 800-8193336 |
| Website: |
https://www.sigmaaldrich.cn |
| Company Name: |
skychemical Co.Ltd
|
| Tel: |
021-20960837,QQ1332204249 |
| Website: |
http://www.skychemical.com |
|