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品質等級
化驗
96%
反應適用性
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: ligand
折射率
n20/D 1.546 (lit.)
bp
120-121 °C/29 mmHg (lit.)
密度
0.954 g/mL at 25 °C (lit.)
官能基
phosphine
SMILES 字串
CCP(CC)c1ccccc1
InChI
1S/C10H15P/c1-3-11(4-2)10-8-6-5-7-9-10/h5-9H,3-4H2,1-2H3
InChI 密鑰
LVTCZSBUROAWTE-UHFFFAOYSA-N
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應用
Catalyst for:
- Selective cross-dimerization
- Diastereoselective condensations
- Carboxyl migration reactions
- Selective hydrogenation
- Asymmetric induction by chiral diphosphines in ring contraction
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
183.2 °F - closed cup
閃點（°C）
84 °C - closed cup
個人防護裝備
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
B P Smyser et al.
Biochemical pharmacology, 35(10), 1719-1723 (1986-05-15)
Purified mouse liver cytochrome P-450 reconstituted with purified NADPH-cytochrome P-450 reductase and phosphatidylcholine metabolized diethylphenylphosphine to diethylphenylphosphine oxide. NADPH was required for the reaction and the amount of oxide formed was time and cytochrome P-450 dependent. Purified phenobarbital-induced cytochrome P-450
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