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2,3,6,7-Tetrakis(benzoylthio)tetrathiafulvalene (TBTT) is an organic compound with a distinctive molecular structure that comprises four thiafulvalene units interconnected by four benzoylthio groups. This electron-rich chemical is recognized for its exceptional conductivity and has been extensively utilized as a fundamental component in the creation of conductive materials and organic electronic devices. TBTT's unique structural and electronic characteristics render it a highly valuable asset for the progress of organic electronics and materials science.

88203-73-0

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88203-73-0 Usage

Uses

Used in Organic Electronics:
2,3,6,7-Tetrakis(benzoylthio)tetrathiafulvalene is used as a conductive material for its electron-rich nature, which contributes to the development of organic electronic devices.
Used in Organic Photovoltaics:
2,3,6,7-Tetrakis(benzoylthio)tetrathiafulvalene is used as a key component in the construction of organic photovoltaics, where its conductivity plays a crucial role in the efficiency of solar energy conversion.
Used in Organic Field-Effect Transistors:
2,3,6,7-Tetrakis(benzoylthio)tetrathiafulvalene is used as a semiconductor material in organic field-effect transistors, leveraging its electronic properties to control the flow of current.
Used in Molecular Wires:
2,3,6,7-Tetrakis(benzoylthio)tetrathiafulvalene is used as a molecular wire, facilitating the transfer of electrical charge between molecules, which is essential for the miniaturization of electronic components.

Check Digit Verification of cas no

The CAS Registry Mumber 88203-73-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,0 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88203-73:
(7*8)+(6*8)+(5*2)+(4*0)+(3*3)+(2*7)+(1*3)=140
140 % 10 = 0
So 88203-73-0 is a valid CAS Registry Number.

88203-73-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,6,7-Tetrakis(benzoylthio)tetrathiafulvalene

1.2 Other means of identification

Product number -
Other names tetrabenzoylthiotetrathiafulvalene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:88203-73-0 SDS

88203-73-0Downstream Products

88203-73-0Relevant academic research and scientific papers

2-(Triphenylphosphonio)-4,5-bis(benzoylthio)-1,3-dithiole Tetrafluoroborate: A Versatile Wittig Reagent for the Synthesis of Unsymmetrical Tetrathiafulvalenes and 1,3-Dithiol-2-ylidene Derivatives

Hansen, Thomas K.,Bryce, Martin R.,Howard, Judith A. K.,Yufit, Dimitri S.

, p. 5324 - 5327 (2007/10/02)

The title Wittig reagent 5 has been prepared in three steps (84percent overall yield) from 4,5-bis(benzoylthio)-1,3-dithiole-2-thione.Reactions of ylide 7, generated by treatment of 5 with diisopropylethylamine at room temperature, have been exploited in the synthesis of new unsymmetrical tetrathiafulvalenes and 1,3-dithiol-2-ylidene derivatives.Subsequent removal of the benzoyl protecting group with sodium ethoxide liberates the transient TTF-dithiolate or 1,3-dithiole-dithiolate anions which can be alkylated in situ.The X-ray crystal structures of compounds 17 and 18 are reported: close nonbonded S...O intramolecular interactions are observed in both structures.

Improved Synthesis and Crystal Structure of Tetrakis(benzoylthio)tetrathiafulvalene. A Useful Precursor to Functionalised Bis(ethylenedithio)tetrathiafulvalene Derivatives

Hansen, Thomas K.,Hawkins, Ian,Varma, K. Sukumar,Edge, Stephen,Larsen, Sine,et al.

, p. 1963 - 1966 (2007/10/02)

A simple one-step procedure is reported for the preparation of tetrakis(benzoylthio)tetrathiafulvalene (2) using octacarbonyldicobalt.The crystal structure of 2 is discussed and the preparation of some charge-transfer salts of 2 and their electrical condu

Tetrathiafulvalenes. XIX. Synthesis and Properties of Electron Conducting Poly-Dithiolene Complexes with Ethylene Tetrathiolat and Tetrathiafulvalene Tetrathiolat as Bridge Ligands

Poleschner, H.,John, W.,Hoppe, F.,Fanghaenel, E.

, p. 957 - 975 (2007/10/02)

-Dithiolo-1,3-dithiol-2,5-dione 7 and 5-(5-oxo-dithiolo-1,3-dithiole-2-ylidene)-dithiolo-1,3-dithiol-2-one 8 were synthesized from 1,3-dithiole-2-thione-4,5-dithiolat.The ligands react with salts of iron, cobalt, nickel

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