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Merck
CN

261939

1,2-Bis(dimethylphosphino)ethane

97%, liquid

Synonym(s):

DMPE, Dimethyl-2-(dimethylphosphino)ethylphosphine, Ethylenebis(dimethylphosphine)

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About This Item

Linear Formula:
(CH3)2PCH2CH2P(CH3)2
CAS Number:
Molecular Weight:
150.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352001
MDL number:
Beilstein/REAXYS Number:
1732994
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Product Name

1,2-Bis(dimethylphosphino)ethane, 97%

InChI

1S/C6H16P2/c1-7(2)5-6-8(3)4/h5-6H2,1-4H3

SMILES string

CP(C)CCP(C)C

InChI key

ZKWQSBFSGZJNFP-UHFFFAOYSA-N

assay

97%

form

liquid

reaction suitability

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

refractive index

n20/D 1.507 (lit.)

bp

180 °C (lit.)

density

0.9 g/mL at 25 °C (lit.)

functional group

phosphine

Quality Level

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Application

1,2-Bis(dimethylphosphino)ethane (dmpe) may be employed as ligand in the preparation of cis-arylmethyl(dmpe) nickel(II) complexes.

General description

1,2-Bis(dimethylphosphino)ethane (dmpe) is a polydentate phosphine ligand. Synthesis of 1,2-bis(dimethylphosphino)ethane has been reported. It reacts with ZrCl2 to afford ZrCl4(dmpe)2 complexes.

pictograms

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Danger

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 3

ppe

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

Regulatory Information

监管及禁止进口产品
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A convenient synthesis of 1, 2-bis (dichlorophosphino) ethane, 1, 2-bis (dimethylphosphino) ethane and 1,2-bis (diethylphosphino) ethane.
Burt RJ, et al.
Journal of Organometallic Chemistry, 182(2), 203-206 (1979)
Phosphine-induced reductive elimination from cis-arylmethylnickel (II) complexes having a 1,2-bis(dimethylphosphino) ethane ligand
Komiya S, et al.
Organometallics, 2(10), 1466-1468 (1983)
Beatty RP, et al.
Inorganic Chemistry, 18(11), 3139-3145 (1979)
M Suwalsky et al.
Biochimica et biophysica acta, 1848(11 Pt A), 2829-2838 (2015-08-25)
Usnic acid (UA) has been associated with chronic diseases through its antioxidant action. Its main target is the cell membrane; however, its effect on that of human erythrocytes has been scarcely investigated. To gain insight into the molecular mechanisms of
Mario Suwalsky et al.
The Journal of membrane biology, 248(4), 683-693 (2015-03-01)
Despite the extended use and well-documented information, there are insufficient reports concerning the effects of propranolol on the structure and functions of cell membranes, particularly those of human erythrocytes. Aimed to better understand the molecular mechanisms of its interactions with

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