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Tungsten, pentacarbonyl(triethylphosphine)-, also known as (triethylphosphine)pentacarbonyltungsten, is a chemical compound with the formula W(CO)5(PEt3). It is a derivative of tungsten hexacarbonyl, where one carbonyl ligand is replaced by a triethylphosphine ligand. Tungsten, pentacarbonyl(triethylphosphine)- is an organometallic complex, which means it contains a metal (tungsten) bonded to carbon-containing ligands. It is used as a catalyst in various chemical reactions, particularly in the field of homogeneous catalysis. The compound is sensitive to air and moisture, and it is typically handled under an inert atmosphere. Its structure and reactivity make it a valuable tool in the synthesis of complex organic molecules and in the study of metal-ligand interactions.

21321-31-3

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21321-31-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21321-31-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,3,2 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 21321-31:
(7*2)+(6*1)+(5*3)+(4*2)+(3*1)+(2*3)+(1*1)=53
53 % 10 = 3
So 21321-31-3 is a valid CAS Registry Number.

21321-31-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[1,4-dioxobuta-1,3-dien-2-yl-ethyl-(oxomethylidene)-λ<sup>5</sup>-phosphanyl]buta-1,3-diene-1,4-dione,tungsten

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:21321-31-3 SDS

21321-31-3Downstream Products

21321-31-3Relevant academic research and scientific papers

Generation and spectroscopic observation of a tungsten-carbene-alkene intermediate in cyclopropane formation

Casey, Charles P.,Shusterman, Alan J.

, p. 736 - 744 (1985)

The alkoxide-catalyzed reaction of but-3-en-1-ol with (CO)5W=C(OCH3)C6H4-p-CH3 gives the (butenyloxy)carbene complex (CO5)W=C(OCH2CH2CH=CH2)C 6H4-p-CH3, 1, which possesses a carbene ligand and an uncomplexed alkene. Upon heating at 38°C in benzene-d6, 1 is converted to the cyclopropane 1-(4-methylphenyl)-2-oxabicyclo[3.1.0]hexane, 10. During the conversion of 1 to 10, an intermediate tetracarbonyltungsten-carbene-alkene complex 15 was detected by 1H NMR and IR spectroscopy. Intermediate 15 reacted with CO to regenerate 1 and with PEt3 to give cis-(CO)4(PEt3)W=C-(OCH2CH 2CH=CH2)C6H4-p-CH3,18. The kinetics of the conversion of 1 to 10 are very complex. After an initial induction period, an accelerating autocatalytic decomposition of 1 occurs. A detailed mechanism for the autocatalysis is proposed in which the key steps are decomposition of tungsten-carbene-alkene intermediate 15 which reacts successively with two molecules of starting material 1 to generate W(CO)6 and 2 equiv of tungsten-carbene-alkene intermediate 15.

Structural Differences in η5-C5H5 and η5-P3C2But2 Tetrametallic Complexes. Synthesis of t2)(CO)8(PEt3)2> and t2)2(CO)6(PEt3)2>, (M= Cr, Mo, W). Crystal and Molecular Structure of

Hitchcock, Peter B.,Meidine, Mohamed F.,Nixon, John F.,Sillet, Gary J.D.

, p. 317 - 319 (2007/10/02)

The two tetrametallic complexes and 5-P3C2But2)2(CO)6(PEt3)2> have copletely different molecular structures.

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