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Merck

324108

Sigma-Aldrich

Trimethylphosphine solution

1.0 M in THF

Sinónimos:

PMe3, Trimethylphosphorus

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About This Item

Fórmula lineal:
(CH3)3P
Número de CAS:
Peso molecular:
76.08
Beilstein/REAXYS Number:
969138
MDL number:
UNSPSC Code:
12352128
PubChem Substance ID:
NACRES:
NA.22

form

liquid

Quality Level

reaction suitability

reagent type: ligand
reaction type: Mitsunobu Reaction

reagent type: ligand
reaction type: Wittig Reaction

concentration

1.0 M in THF

density

0.872 g/mL at 25 °C

functional group

phosphine

SMILES string

CP(C)C

InChI

1S/C3H9P/c1-4(2)3/h1-3H3

InChI key

YWWDBCBWQNCYNR-UHFFFAOYSA-N

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General description

Trimethylphosphine is the reagent used in Mitsunobu reaction. It participates in the transformation of azides into carbamates, aziridines from azidoalcohols, iminophosphoranes and aza-Wittig reaction. Electron diffraction study of trimethylphosphine has been reported.

Application

Trimethylphosphine (PMe3) solution is the suitable reagent used in the synthesis of Fe/Te cluster type complex, Fe6Te8(PMe3)6. It may be employed as a probe to investigate the acid sites in Y-zeolite. It may be used for the synthesis of hexakis(trimethylphosphine)tris-μ-methylene-diruthenium(III).

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Referencia del producto
Descripción
Precios

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Central nervous system, Respiratory system

supp_hazards

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

-22.0 °F - closed cup

flash_point_c

-30 °C - closed cup

ppe

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


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Synthesis and x-ray crystal structures of hexakis (trimethylphosphine) tris-. mu.-methylene-diruthenium (III) and its mono-and dicationic derivatives.
Hursthouse MB, et al.
Journal of the American Chemical Society, 101(15), 4128-4139 (1979)
Electron diffraction study of the structure of trimethylphosphine.
Bartell LS and Brockway LO.
J. Chem. Phys. , 32(2), 512-515 (1960)
Acid sites in zeolite Y: a solid-state NMR and infrared study using trimethylphosphine as a probe molecule.
Lunsford JH, et al.
Journal of the American Chemical Society, 107(6), 1540-1547 (1985)
Effect of Diverse Ligands on the Course of a Molecules-to-Solids Process and Properties of Its Intermediates.
Steigerwald ML, et al.
Inorganic Chemistry, 33(15), 3389-3395 (1994)
Raúl García-Rodríguez et al.
Journal of the American Chemical Society, 134(3), 1400-1403 (2012-01-10)
We outline a reaction pathway for the cleavage of the P═Se bond in trialkylphosphine selenide during the synthesis of CdSe nanocrystals. The reaction between cadmium carboxylate and trimethylphosphine selenide in the presence of an alcohol produces alkoxytrimethylphosphonium (2). Control experiments

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