tert-Butylferrocene

95%

Reagent Code: #143704
label
Alias tert-butyl ferrocene
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CAS Number 1316-98-9

science Other reagents with same CAS 1316-98-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.14 g/mol
Formula Fe(C₅H₅)(C₅H₄C(CH₃)₃)
badge Registry Numbers
MDL Number MFCD00058729
thermostat Physical Properties
Boiling Point 96°C (1 mmHg)
inventory_2 Storage & Handling
Density 1.201
Storage Room temperature, dry

description Product Description

Used as a redox-active building block in organometallic chemistry, particularly in the development of electroactive materials and sensors. Its stable ferrocene core with a bulky tert-butyl group enhances solubility in organic solvents and improves performance in thin-film applications such as molecular electronics and electrochemical detectors. Commonly employed in the synthesis of functionalized metallocenes for catalysis and in designing redox mediators in bioelectrochemistry. Also finds use in studying steric effects on electron transfer processes due to the electron-donating nature of the tert-butyl substituent.

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inventory 1g
10-20 days ฿5,020.00

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tert-Butylferrocene
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Used as a redox-active building block in organometallic chemistry, particularly in the development of electroactive materials and sensors. Its stable ferrocene core with a bulky tert-butyl group enhances solubility in organic solvents and improves performance in thin-film applications such as molecular electronics and electrochemical detectors. Commonly employed in the synthesis of functionalized metallocenes for catalysis and in designing redox mediators in bioelectrochemistry. Also finds use in studyin

Used as a redox-active building block in organometallic chemistry, particularly in the development of electroactive materials and sensors. Its stable ferrocene core with a bulky tert-butyl group enhances solubility in organic solvents and improves performance in thin-film applications such as molecular electronics and electrochemical detectors. Commonly employed in the synthesis of functionalized metallocenes for catalysis and in designing redox mediators in bioelectrochemistry. Also finds use in studying steric effects on electron transfer processes due to the electron-donating nature of the tert-butyl substituent.

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