ChemicalBook > Product Catalog > Organic Chemistry > Organometallic compounds > Organic iron > Vinylferrocene
Vinylferrocene
Vinylferrocene Basic information
- Product Name:
- Vinylferrocene
- Synonyms:
-
- Ferrocene, ethenyl-
- VINYLFERROCENE
- Vinylferroceneorangextl
- Vinylferrocene,98%
- Vinylferrocene ,97%
- Vinylferrocene**CUSTOMSYNTHESISPLEASEASK**
- Vinylferrocene,99%
- Vinylferrocene 97%
- CAS:
- 1271-51-8
- MF:
- C12H12Fe10*
- MW:
- 212.07
- EINECS:
- 215-041-1
- Product Categories:
-
- metallocene
- Classes of Metal Compounds
- Fe (Iron) Compounds
- Ferrocenes
- Metallocenes
- Transition Metal Compounds
- Catalysis and Inorganic Chemistry
- Chemical Synthesis
- Mol File:
- 1271-51-8.mol
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Vinylferrocene Chemical Properties
- Melting point:
- 51-53 °C (lit.)
- Boiling point:
- 80-85 °C/0.2 mmHg (lit.)
- Flash point:
- 144 °F
- storage temp.
- Sealed in dry,2-8°C
- form
- crystal
- color
- orange
- Water Solubility
- Insoluble in water.
- Hydrolytic Sensitivity
- 4: no reaction with water under neutral conditions
- Exposure limits
- ACGIH: TWA 1 mg/m3
NIOSH: TWA 1 mg/m3 - Stability:
- Stable. Highly flammable. Incompatible with strong acids, strong oxidizing agents.
- NIST Chemistry Reference
- Vinylferrocene(1271-51-8)
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Safety Information
- Hazard Codes
- F
- Risk Statements
- 11-22
- Safety Statements
- 16-22-24/25-7/9-33
- RIDADR
- UN 1325 4.1/PG 2
- WGK Germany
- 3
- F
- 10
- TSCA
- No
- HazardClass
- 4.1
- PackingGroup
- II
- HS Code
- 29319090
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
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Vinylferrocene Usage And Synthesis
Chemical Properties
crystalline solid
Uses
Used in the synthesis of 2-aminomethylferrocenes from vinyl ferrocene and lithium amides.
Definition
ChEBI: Ferrocene substituted on one of the cyclopentadienyl rings by a vinyl group.
Purification Methods
Dissolve vinylferrocene in Et2O, wash it with H2O and brine, dry (Na2SO4), and evaporate to a small volume. Purify it through an Al2O3 (Spence grade H) column by eluting the yellow band with pet ether (b 40-60o). The low melting orange crystals can be sublimed. The tetracyanoethylene adduct crystallises from *C6H6/pentane and has m 137-139o(dec). [Horspool & Sutherland Can J Chem 46 3453 1968, Berger et al. J Org Chem 39 377 1974, Rauch & Siegel J Organomet Chem 11 317 1968, Beilstein 16 III 1787.]
Vinylferrocene Preparation Products And Raw materials
Raw materials
VinylferroceneSupplier
Wuhan Pengo Technology.,Ltd. Gold
- Tel
- 027-60707801 13628634921
- sunny.w@boronicgroup.com
Hubei Xishaonian biotechnology co., ltd Gold
- Tel
- 0711-3700636 18827410479
- xujin@boronicgroup.com
Shandong Lingqing Pharmaceutical Technology Co., Ltd. Gold
- Tel
- 18600392407 18668996177
- linkingpharm@126.com
J & K SCIENTIFIC LTD.
- Tel
- 010-82848833 400-666-7788
- jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
- Tel
- 021-61259108 18621169109
- market03@meryer.com
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Vinylferrocene(1271-51-8)Related Product Information
- Ethylferrocene
- Aminoferrocene
- tert-Butylferrocene
- ETHYNYLFERROCENE
- Acetylferrocene
- Ferrocenecarboxylic acid
- Ferrocenecarboxaldehyde
- Ferrocene
- Tungsten carbide
- Sodium ethanesulfinate
- Cobalt acetate
- Vinyl silicone oil
- Ethylenesulfonic acid
- n-Butyl vinyl ether
- Ethyl vinyl ether
- 3-methyl-1-(2,6,6-trimethylcyclohex-1-en-1-yl)penta-1,4-dien-3-ol
- Methoxyethene
- Sodium ethylenesulphonate