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Merck
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重要文件

642629

Sigma-Aldrich

二叔丁基甲膦

97%

同義詞:

(t-Bu)2PMe, Bis(tert-butyl)methylphosphine

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About This Item

線性公式:
[(CH3)3C]2PCH3
CAS號碼:
分子量::
160.24
MDL號碼:
分類程式碼代碼:
12352001
PubChem物質ID:
暫時無法取得訂價和供貨情況

品質等級

化驗

97%

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
reaction type: Cross Couplings

bp

58 °C/12 mmHg (lit.)

密度

0.824 g/mL at 25 °C (lit.)

官能基

phosphine

SMILES 字串

CP(C(C)(C)C)C(C)(C)C

InChI

1S/C9H21P/c1-8(2,3)10(7)9(4,5)6/h1-7H3

InChI 密鑰

JURBTQKVGNFPRJ-UHFFFAOYSA-N

應用

在交叉偶联催化反应中与多种钯复合物一起使用的大体积膦。[1]
Di-tert-butylmethylphosphine (PtBu2Me) when added as HBF4 salt, enhances the reactivity of palladium-catalyzed direct arylation of heterocylic arenes with aryl chlorides, bromides[2] and azine N-oxides with aryl triflates to form the corresponding biaryl and 2-aryl azine N-oxides, respectively.[3] It may be used in the preparation of CoCl2(PtBu2Me)2, a cobalt phosphine complex, which in combination with methylaluminoxane (MAO) catalyzes the butadiene polymerization to form predominantly the cis-1,4 polymer.[4]

象形圖

FlameCorrosion

訊號詞

Danger

危險聲明

危險分類

Pyr. Liq. 1 - Skin Corr. 1B

儲存類別代碼

4.2 - Pyrophoric and self-heating hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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Synthesis, structure, and butadiene polymerization behavior of alkylphosphine cobalt (II) complexes.
Ricci G, et al.
J. Mol. Catal. A: Chem., 226(2), 235-241 (2005)
Catalytic direct arylation with aryl chlorides, bromides, and iodides: intramolecular studies leading to new intermolecular reactions.
Campeau LC, et al.
Journal of the American Chemical Society, 128(2), 581-590 (2006)
Jae-Young Lee et al.
Journal of the American Chemical Society, 125(19), 5616-5617 (2003-05-08)
The first method for achieving Hiyama couplings of unactivated alkyl bromides and iodides is reported. The desired carbon-carbon bond formation proceeds under mild conditions (room temperature) with good functional-group tolerance.
Direct arylation of azine N-oxides with aryl triflates.
Schipper DJ, et al.
Tetrahedron, 65(26), 4977-4983 (2009)

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