11-Ferrocenyl-1-undecanethiol

• CAS: 127087-36-9
• Catalog Number: ACM127087369-2
• Category: Biomaterials
• Molecular Weight: 372.4
• Molecular Formula: C21H32FeS
• Description: 11-Ferrocenyl-1-undecanethiol (11-FUDT) is an organosulfur compound consisting of an alkyl chain with a ferrocene group at the end. It is a relatively new compound with a wide range of applications in the scientific research community. It is a promising material for use in various scientific experiments due to its unique properties and its ability to be synthesized in a variety of ways. 11-FUDT has been studied extensively and has been found to have numerous biochemical and physiological effects.
• Synonyms: 11-Ferrocenyl-1-Undecanethiol;11-(Ferrocenyl)undecanethiol;11-(Mercaptoundecyl)ferrocene
• IUPAC Name: cyclopenta-1,3-diene;11-cyclopenta-1,4-dien-1-ylundecane-1-thiol;iron(2+)
• Canonical SMILES: [CH-]1C=CC=C1.[CH-]1C=CC(=C1)CCCCCCCCCCCS.[Fe+2]
• InChI: InChI=1S/C16H27S.C5H5.Fe/c17-15-11-7-5-3-1-2-4-6-8-12-16-13-9-10-14-16;1-2-4-5-3-1;/h9-10,13-14,17H,1-8,11-12,15H2;1-5H;/q2*-1;+2
• InChI Key: JKOWKXHCMQEEQQ-UHFFFAOYSA-N
• Melting Point: 36-41 °C
• Application: 11-Ferrocenyl-1-undecanethiol has a wide range of applications in scientific research. It has been used in a variety of experiments to investigate the biochemical and physiological effects of the compound. It has also been used to study the effects of various drugs and other compounds on cells and tissues. 11-Ferrocenyl-1-undecanethiol has also been used in the development of new drugs and other compounds.
• Storage: Store at 2-8 ℃
• Complexity: 161
• Covalently-Bonded Unit Count: 3
• Exact Mass: 372.157
• Formal Charge: 0
• Hazard Statements: H315-H319-H335
• H-Bond Acceptor: 3
• H-Bond Donor: 1
• Heavy Atom Count: 23
• MDL Number: MFCD20264873
• Monoisotopic Mass: 372.157408
• PSA: 38.8
• Rotatable Bond Count: 11
• Supplemental Hazard Statements: H315-H319-H335
• Symbol: GHS07
• WGK Germany: 3
• XLogP3: 6.8319

Case Study

Molecular Probe Constructed from 11-Ferrocenyl-1-Undecanethiol for Electrochemical Research

Wong, Raymond A., et al. Nature Communications, 2020, 11(1): 4194.

Ferrocene-terminated alkanethiol self-assembled monolayers (Fc SAM) on gold can serve as attractive molecular probes for studies related to interfacial electrochemistry and interface physicochemical properties. This molecular probe can be used to explore how electrochemical responses are transformed based on the electronic and structural properties of the electrode/monolayer/electrolyte interface.
Preparation of monolayers based on 11-ferrocenyl-1-undecanethiol
· The clean Au substrates were immersed for at least 12 h in ethanol solutions containing 0.1 mM 11-ferrocenyl-1-undecanethiol followed by rinsing with ethanol and drying under a stream of N2 gas.
· For the mixed SAM/dilution experiments, an as-prepared SAM from 1 mM 1-decanethiol in ethanol was subsequently submerged in 0.1 mM 11-ferrocenyl-1-undecanethiol (in ethanol) for at least 30 mins followed by rinsing with ethanol and drying under a stream of N2 gas.

Preparation of ZnO Nanowire/11-Ferrocenyl-1-Undecanethiol Arrays for Efficient Glucose Sensing

Tao, Bairui, et al. Int. J. Electrochem. Sci, 2017, 12, 7216-7226.

A one-dimensional ZnO nanowire/ferrocenyl alkanethiol array can be synthesized on a silicon substrate via self-assembly and low-temperature aqueous method. The ZnO NWs/FcC11SH/Si array was further immobilized with glucose oxidase to obtain GOx/ZnO NWs/FcC11SH/Si, which has excellent electrocatalytic activity for glucose, which can be used in clinical, environmental and food analysis.
· Self-assembling of 11-ferrocenyl-1-undecanethiol
A 30 nm Ti layer and 100 nm Au layer was deposited on the surface of silicon by thermal evaporation, respectively. The as-prepared substrates were immersed in a 10 mM ethanol solution of 11-ferrocenyl-1-undecanethiol (FcC11SH) for 24 h. After self-assembling, the electrode was rinsed with ethanol and deionized water several times.
· Synthesis of ZnO NWs/FcC11SH/Si array
ZnO seed layers were prepared by spin coating and then annealed at 350 ◦C for 30 min in ambient air for growth the NWs arrays. Zn (CH3COO) 2·2H2O, NH3·H2O were mixed in distilled water with a well stirred. Then put the above substrate with ZnO seed layer in this reaction solution for 2 h at 80 °C.

Custom Q&A

What is the molecular formula of 11-Ferrocenyl-1-undecanethiol?

The molecular formula of 11-Ferrocenyl-1-undecanethiol is C21H32FeS.

What is the molecular weight of 11-Ferrocenyl-1-undecanethiol?

The molecular weight of 11-Ferrocenyl-1-undecanethiol is 372.4 g/mol.

What is the IUPAC name of 11-Ferrocenyl-1-undecanethiol?

The IUPAC name of 11-Ferrocenyl-1-undecanethiol is cyclopenta-1,3-diene;11-cyclopenta-1,3-dien-1-ylundecane-1-thiol;iron(2+).

What is the InChI of 11-Ferrocenyl-1-undecanethiol?

The InChI of 11-Ferrocenyl-1-undecanethiol is InChI=1S/C16H27S.C5H5.Fe/c17-15-11-7-5-3-1-2-4-6-8-12-16-13-9-10-14-16;1-2-4-5-3-1;/h9-10,13-14,17H,1-8,11-12,15H2;1-5H;/q2*-1;+2.

What is the InChIKey of 11-Ferrocenyl-1-undecanethiol?

The InChIKey of 11-Ferrocenyl-1-undecanethiol is JKOWKXHCMQEEQQ-UHFFFAOYSA-N.

What is the canonical SMILES of 11-Ferrocenyl-1-undecanethiol?

The canonical SMILES of 11-Ferrocenyl-1-undecanethiol is [CH-]1C=CC=C1.[CH-]1C=CC=C1CCCCCCCCCCCS.[Fe+2].

What is the CAS number of 11-Ferrocenyl-1-undecanethiol?

The CAS number of 11-Ferrocenyl-1-undecanethiol is 127087-36-9.

What is the European Community (EC) number of 11-Ferrocenyl-1-undecanethiol?

The European Community (EC) number of 11-Ferrocenyl-1-undecanethiol is 687-881-0.

What is the hydrogen bond donor count of 11-Ferrocenyl-1-undecanethiol?

The hydrogen bond donor count of 11-Ferrocenyl-1-undecanethiol is 1.

What is the hydrogen bond acceptor count of 11-Ferrocenyl-1-undecanethiol?

The hydrogen bond acceptor count of 11-Ferrocenyl-1-undecanethiol is 3.