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Key Documents

695157

Sigma-Aldrich

双(3,5-二甲苯基)磷

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About This Item

經驗公式(希爾表示法):
C16H19P
CAS號碼:
分子量::
242.30
MDL號碼:
分類程式碼代碼:
12352103
PubChem物質ID:
NACRES:
NA.22

形狀

liquid

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 1.599

密度

1.017 g/mL at 25 °C

官能基

phosphine

SMILES 字串

Cc1cc(C)cc(Pc2cc(C)cc(C)c2)c1

InChI

1S/C16H19P/c1-11-5-12(2)8-15(7-11)17-16-9-13(3)6-14(4)10-16/h5-10,17H,1-4H3

InChI 密鑰

GPFIUEZTNRNFGD-UHFFFAOYSA-N

應用

Bis(3,5-dimethylphenyl)phosphine can be used as a reactant to prepare:
  • Iron(II) chiral diimine diphosphine complexes as catalysts for the asymmetric transfer hydrogenation of ketones.
  • The complex of iridium with biphenol phosphite-phosphine bidentate ligand as an asymmetric catalyst for the hydrogenation of N-arylimines.
  • Chiral phosphines with excellent stereoselectivity by 1, 4 addition reaction with α,β-unsaturated aldehydes using a palladium catalyst.

法律資訊

Kanata Chemical Technologies, Inc. 产品

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

>230.0 °F

閃點(°C)

> 110 °C

個人防護裝備

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


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分析證明 (COA)

Lot/Batch Number

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存取文件庫

Palladium-catalyzed 1, 4-addition of diarylphosphines to α, β -unsaturated aldehydes
Chen Y-R and Duan W-L
Organic Letters, 13(21), 5824-5826 (2011)
Stereoelectronic factors in iron catalysis: synthesis and characterization of aryl-substituted iron (II) carbonyl P-N-N-P complexes and their use in the asymmetric transfer hydrogenation of ketones
Sues PE, et al.
Organometallics, 30(16), 4418-4431 (2011)

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