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Vanadinocene Dichloride

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Vanadinocene Dichloride Basic information

Product Name:
Vanadinocene Dichloride
Synonyms:
  • dichlorodi-pi-cyclopentadienyl-vanadiu
  • Bis(cyclopentadienyl)vanadium dichloride (Vanadocene dichloride),98%
  • Dicyclopentadienevanadium dichloride
  • Dicyclopentadienyldichlorovanadium
  • Bis(cyclopentadienyl)vanadiuM dichloride, 95% 1GR
  • Dichlorobis(cyclopentadienyl)vanadium
  • Bis(cyclopentadienyl)vanadium(IV) dichloride 95%
  • Bis(cyclopentadienyl)vanadium dichloride, 98% (Vanadocene dichloride)
CAS:
12083-48-6
MF:
C10H10Cl2V10*
MW:
252.03
EINECS:
235-150-8
Product Categories:
  • metallocene
  • Transition Metal Compounds
  • V (Vanadium) Compounds
  • Catalysis and Inorganic Chemistry
  • Chemical Synthesis
  • Vanadium
  • Classes of Metal Compounds
  • Metallocenes
  • Titanocene, etc.
Mol File:
12083-48-6.mol
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Vanadinocene Dichloride Chemical Properties

Melting point:
182-194 °C (dec.)(lit.)
Density 
1,6 g/cm3
storage temp. 
2-8°C
solubility 
soluble in H2O, chloroform, ethanol
form 
crystal
Specific Gravity
1.6
color 
green
Water Solubility 
Reacts with water
Sensitive 
Air & Moisture Sensitive
Exposure limits
NIOSH: Ceiling 0.05 mg/m3
CAS DataBase Reference
12083-48-6(CAS DataBase Reference)
EPA Substance Registry System
Vanadocene dichloride (12083-48-6)
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Safety Information

Hazard Codes 
T
Risk Statements 
25-36/37/38
Safety Statements 
26-28-36/37/39-45
RIDADR 
UN 3285 6.1/PG 3
WGK Germany 
3
RTECS 
YW1580000
HazardClass 
8
PackingGroup 
II
HS Code 
29310099

MSDS

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Vanadinocene Dichloride Usage And Synthesis

Chemical Properties

dark green crystalline powder

Uses

Vanadocene dichloride is used like other metallocenes as a catalyst, ultraviolet absorber, reducing agent, free radical scavenger, antiknock agent in gasoline, and as a developmental anticancer drug.

Uses

Bis(cyclopentadienyl)vanadium(IV) dichloride is a catalyst for solvent free, room temperature preparation of vicinal amino alcohols as fungistatic agents, catalyst fot oligomerization reactions via the Aufbau propagation reaction and as a catalyst for aqueous polymerization reactions using oxygen as a co catalyst. It is used as a catalyst for dl-selective pinacol-type coupling reactions, as an affecter of crystal growth of calcium carbonate and and as an inhibitor of human topoisomerase II enzyme with antitumor activity.

General Description

Pale green crystals or green powder.

Air & Water Reactions

Extremely sensitive to exposure to air. Also extremely sensitive to moisture; decomposes in water

Reactivity Profile

Organometallics, such as BIS(CYCLOPENTADIENYL)VANADIUM DICHLORIDE, are reactive with many other groups. Incompatible with acids and bases. Organometallics are good reducing agents and therefore incompatible with oxidizing agents. Often reactive with water to generate toxic or flammable gases. Organometallics containing halogens (fluorine, chlorine, bromine, iodine) bonded to the metal typically with generate gaseous hydrohalic acids (HF, HCl, HBr, HI) with water.

Fire Hazard

Flash point data for BIS(CYCLOPENTADIENYL)VANADIUM DICHLORIDE are not available. BIS(CYCLOPENTADIENYL)VANADIUM DICHLORIDE is probably combustible.

Pharmaceutical Applications

Vanadocene dichloride [( η5-C5H5)2VCl2, dichloro bis(η5-cyclopentadienyl)vanadium(IV)] is structurally very similar to Cp2TiCl2. It also consists of a metal centre with an oxidation number of +IV, in this case vanadium, and two Cp and two chloride ligands. Vanadocene dichloride is a 17-electron complex containing an unpaired electron and is therefore paramagnetic .
Vanadocene dichloride has found application as a catalyst for polymerisation reactions, but was also intensively studied as an anticancer agent in parallel to Cp2TiCl2 because of their structural similarities. Vanadocene dichloride has proven to be even more effective than its titanium analogue as an antiproliferative agent against both animal and human cell lines in preclinical testing. The main problems are the difficult characterisation of the active vanadium compounds and their fast hydrolysis.

Pharmaceutical Applications

Vanadocene dichloride [(η5-C5H5)2VCl2, dichloro bis(η5-cyclopentadienyl)vanadium(IV)] is structurally very similar to Cp2TiCl2. It also consists of a metal centre with an oxidation number of +IV, in this case vanadium, and two Cp and two chloride ligands. Vanadocene dichloride is a 17-electron complex containing an unpaired electron and is therefore paramagnetic. Vanadocene dichloride has found application as a catalyst for polymerisation reactions, but was also intensively studied as an anticancer agent in parallel to Cp2TiCl2 because of their structural similarities. Vanadocene dichloride has proven to be even more effective than its titanium analogue as an antiproliferative agent against both animal and human cell lines in preclinical testing.

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