Chemodex

4,7-Dibromobenzo[c]-1,2,5-thiadiazole

As low as CHF 116.00
In stock
Only %1 left
CDX-D1026-G0055 gCHF 116.00
NEW
 
More Information
Product Details
Synonyms Dibromo BTD
Product Type Chemical
Properties
Formula C6H2Br2N2S
MW 293.97
CAS 15155-41-6
Source/Host Chemicals Synthetic
Purity Chemicals ≥95% (GC)
Appearance White to yellow to red powder or crystal.
Solubility Soluble in chloroform or DMSO (5mg/ml).
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key FEOWHLLJXAECMU-UHFFFAOYSA-N
Smiles BrC1=CC=C(Br)C2=NSN=C21
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +4°C
Handling Advice Keep under inert gas.
Protect from light and oxygen.
Use/Stability Stable for at least 2 years after receipt when stored at +4°C.
Documents
Product Specification Sheet
Datasheet Download PDF
Description
4,7-Dibromobenzo[c]-1,2,5-thiadiazole is the building block or monomer for the synthesis of light-emitting diodes and conducting polymers for organic electronics. It has been used as bulding block for photovoltaic device polymers and organic semiconductors. It is used as an intermediate for the synthesis of poly[N-9'-heptadecanyl-2,7-carbazole-alt-5,5-(4',7'-di-2-thienyl-2',1',3'-benzothiadiazole)] (PCDTBT) and poly[2,1,3-benzothiadiazole-4,7-diyl[4,4-bis(2-ethylhexyl)-4H-cyclopenta[2,1-b:3,4-b']dithiophene-2,6-diyl]] (PCPDTBT). 4,7-Dibromobenzo[c]-1,2,5-thiadiazole functions as an electron-accepting material in organic electronic devices. It acts as a p-type semiconductor, facilitating the transport of positive charge carriers within the device and exhibits high electron mobility and good stability, making it suitable for use in organic field-effect transistors and organic photovoltaic devices.
Product References
(1) J. Kim, et al.; Polymer 51, 390 (2010) | (2) Z.J. Wang, et al.; ChemSusChem 8, 3459 (2015) | (3) M.S. Pavan, et al.; J. Phys. Chem. B 119, 11382 (2015) | (4) F. Lomneck, et al.; Macromol. Rapid Commun. 36, 231 (2015) | (5) S.A.A. Shah, et al.; J. Mat. Sci. Mat. Electr. 27, 4501 (2016) | (6) E.A. Knyazeva & O.A. Rakitin; Chem. Heterocyc. Comp. 53, 855 (2017) | (7) Y. Uozumi & T. Sato; Synfacts 13, 1101 (2017) | (8) A. Sarasola, et al.; JACS 140, 15631 (2018) | (9) Y. Yu, et al.; ACS Omega 3, 16347 (2018)
© 2017 Adipogen Life Sciences. Pictures: © 2012 Martin Oeggerli. All Rights Reserved.