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CYCLOPENTADIENYLMOLYBDENUM TRICARBONYL DIMER

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CYCLOPENTADIENYLMOLYBDENUM TRICARBONYL DIMER Basic information

Product Name:
CYCLOPENTADIENYLMOLYBDENUM TRICARBONYL DIMER
Synonyms:
  • Bis-(cyclopentadienyl)-molybdenum tricarbonyl
  • (Cyclopentadienyl)tricarbonylmolybdenum dimer
  • Bis[(eta5-cyclopentadienyl)tricarbonylmolybdenum]
  • Bis[(pi-cyclopentadienyl)molybdenum tricarbonyl]
  • Bis[tricarbonyl(eta5-cyclopentadienyl)molybdenum]
  • Di(mu-carbonyltetracarbonyl)di(pi-cyclopentadienyl)dimolybdenum
  • Di[(pi-cyclopentadienyl)tricarbonylmolybdenum]
  • Hexacarbonylbis(eta5-cyclopentadienyl)dimolybdenum(i)
CAS:
12091-64-4
MF:
C16H10Mo2O610*
MW:
490.13
EINECS:
235-156-0
Product Categories:
  • Catalysis and Inorganic Chemistry
  • Chemical Synthesis
  • metallocene
  • Molybdenum
  • MolybdenumVapor Deposition Precursors
  • Precursors by Metal
Mol File:
12091-64-4.mol
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CYCLOPENTADIENYLMOLYBDENUM TRICARBONYL DIMER Chemical Properties

Melting point:
222 °C (dec.)(lit.)
form 
crystal
color 
red to purple
Water Solubility 
It is insoluble in water.
Sensitive 
Air Sensitive
Exposure limits
ACGIH: TWA 10 mg/m3; TWA 3 mg/m3
NIOSH: IDLH 5000 mg/m3
InChI
1S/2C5H5.6CO.2Mo/c2*1-2-4-5-3-1;6*1-2;;/h2*1-5H;;;;;;;;
InChIKey
XCUPBPUEWLTPMQ-UHFFFAOYSA-N
SMILES
[Mo][Mo].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[CH]1[CH][CH][CH][CH]1.[CH]2[CH][CH][CH][CH]2
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Safety Information

Hazard Codes 
Xn
Risk Statements 
20/21/22
Safety Statements 
36
RIDADR 
UN3466
WGK Germany 
3
TSCA 
Yes
HazardClass 
6.1
PackingGroup 
II
HS Code 
29319090
Storage Class
11 - Combustible Solids
Hazard Classifications
Acute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral

MSDS

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CYCLOPENTADIENYLMOLYBDENUM TRICARBONYL DIMER Usage And Synthesis

Chemical Properties

red to purple glistening crystals or powder

Uses

It is widely used as a chemical intermediate in the laboratories, manufacture purposes, chemical and pharmaceutical intemediate.

reaction suitability

core: molybdenum
reagent type: catalyst

Synthesis

Tricarbonyl(Η-cyclopentadienyl)manganese dimerization was prepared as follows: tetrahydrofuran (THF, 45 ml) was added to 18.8 mmol of cyclopentadiene, and after cooling to -78 ??C, 12.5 ml (18.8 mmol) of Bu-Li was added drop-wise, and pentamethylcyclopentadienyl lithium was coordinated. Then 5 g (18.8 mmol) of molybdenum hexacarbonyl was added to the substance and heated at reflux for 48 hours, and when the reaction was complete, the mother liquor was cooled to 0 ??C. Separately, 3.2 g (18.8 mmol) of ferrous sulfate (II) was added to a solution comprising a mixture of 100 ml of pure water and 20 ml of acetic acid, and the solution so obtained was added dropwise to the mother liquor. The resulting red solution was made to undergo suction filtration, washing and drying, and the manganese tricarbonyl (Η-cyclopentadienyl)-co-manganese dimer complex was obtained by recrystallization. The yield was 20%.

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