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化驗
97%
形狀
solid
反應適用性
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
mp
244-250 °C
官能基
phosphine
SMILES 字串
C1N2CN3CN1CP(C2)C3
InChI
1S/C6H12N3P/c1-7-2-9-3-8(1)5-10(4-7)6-9/h1-6H2
InChI 密鑰
FXXRPTKTLVHPAR-UHFFFAOYSA-N
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一般說明
應用
- The molecular mechanisms of antimetastatic ruthenium compounds explored through DIGE proteomics.:该研究通过差异凝胶电泳(DIGE)蛋白质组学研究钌化合物的抗转移作用。分析了钌络合物中的1,3,5-三氮杂-7-磷杂金刚烷及其生物作用,说明它的潜在抗癌性(Guidi et al., 2013)。
- Synthesis, antimicrobial and antiproliferative activity of novel silver(I) tris(pyrazolyl)methanesulfonate and 1,3,5-triaza-7-phosphadamantane complexes.:该研究详述含有1,3,5-三氮杂-7-磷杂金刚烷的新型银络合物的合成,评估它们的抗菌和抗增殖活性,说明该化合物可用于生物医学领域(Pettinari et al., 2011)。
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
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The use of amines and phosphines in nucleophilic catalysis is well precedented; however, arguably one of the severe limitations with respect to exploiting the more nucleophilic, yet less basic, phosphine in this regard is its air sensitivity.
The use of amines and phosphines in nucleophilic catalysis is well precedented; however, arguably one of the severe limitations with respect to exploiting the more nucleophilic, yet less basic, phosphine in this regard is its air sensitivity.
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