Date published: 2026-5-1

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2-Bromo-3-(bromomethyl)thiophene (CAS 40032-76-6)

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CAS Number:
40032-76-6
Molecular Weight:
255.96
Molecular Formula:
C5H4Br2S
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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2-Bromo-3-(bromomethyl)thiophene, also known as BBT, is an organic compound characterized by a heterocyclic ring containing sulfur. Moreover, it plays a role in investigating organic reactions and advancing catalyst development. Furthermore, 2-Bromo-3-(bromomethyl)thiophene facilitates the examination of molecular interactions like hydrogen bonding and pi-stacking. Although the exact mechanism of 2-Bromo-3-(bromomethyl)thiophene remains partially elusive, it is thought to function as a Lewis acid, forming complexes with Lewis bases. These complexes then partake in a series of reactions leading to the creation of novel compounds. Additionally, 2-Bromo-3-(bromomethyl)thiophene is believed to possess catalytic properties, thereby facilitating the formation of fresh compounds.


2-Bromo-3-(bromomethyl)thiophene (CAS 40032-76-6) References

  1. Design, synthesis, and biological evaluation of the N-diarylalkenyl-piperidinecarboxylic acid derivatives as GABA uptake inhibitors (I).  |  Zheng, J., et al. 2006. Bioorg Med Chem Lett. 16: 225-7. PMID: 16246548
  2. Synthesis of an organic-soluble π-conjugated [3]rotaxane via rotation of glucopyranose units in permethylated β-cyclodextrin.  |  Terao, J., et al. 2014. Beilstein J Org Chem. 10: 2800-8. PMID: 25550746
  3. Synthetic Utility of Arylmethylsulfones: Annulative π-Extension of Aromatics and Hetero-aromatics Involving Pd(0)-Catalyzed Heck Coupling Reactions.  |  Sankar, E., et al. 2017. J Org Chem. 82: 13583-13593. PMID: 29134811
  4. Synthesis and Thermal Investigations of Eleven-Membered Ring Systems Containing One of the Heavier Group 14 Element Atoms Si, Ge, and Sn.  |  Eleya, N., et al. 2020. Molecules. 25: PMID: 31936773
  5. Thiophene α-Chain-End-Functionalized Oligo(2-methyl-2-oxazoline) as Precursor Amphiphilic Macromonomer for Grafted Conjugated Oligomers/Polymers and as a Multifunctional Material with Relevant Properties for Biomedical Applications.  |  Bendrea, AD., et al. 2022. Int J Mol Sci. 23: PMID: 35886844
  6. Regioregular poly (thiophene-3-alkanoic acid) s: water soluble conducting polymers suitable for chromatic chemosensing in solution and solid state  |  Ewbank, P. C., Loewe, R. S., Zhai, L., Reddinger, J., Sauvé, G., & McCullough, R. D. 2004. Tetrahedron. 60(49): 11269-11275.
  7. Polythiophenes containing oligo (oxyethylene) side chains as a thin film on a ZnSe single crystal surface  |  van Beek, R., Jenneskens, L. W., Zdravkova, A. N., van der Eerden, J. P., & van Walree, C. A. 2005. Macromolecular Chemistry and Physics. 206(10): 1006-1014.
  8. Main chain polymeric metal complexes based on linkage fluorenevinylene or phenylenevinylene with thienyl (8‐hydro xyquinoline)–cadmium (II) complexes as dye sensitizer for dye‐sensitized solar cells  |  Jin, X., Yu, X., Zhang, W., Zhou, J., Tang, G., & Zhong, C. 2013. Journal of Applied Polymer Science. 129(6): 3104-3112.
  9. Bithiophene with Winding Vine-shaped Molecular Asymmetry. Preparation, Structural Characterization, and Enantioselective Synthesis  |  Toyomori, Y., Tsuji, S., Mitsuda, S., Okayama, Y., Ashida, S., Mori, A.,.. & Ogasawara, M. 2016. Bulletin of the Chemical Society of Japan. 89(12): 1480-1486.
  10. Fine-tuning the solid-state ordering and thermoelectric performance of regioregular P3HT analogues by sequential oxygen-substitution of carbon atoms along the alkyl side chains  |  Chen, L., Liu, W., Yan, Y., Su, X., Xiao, S., Lu, X.,.. & Tang, X. 2019. Journal of Materials Chemistry C. 7(8): 2333-2344.
  11. A study on regulating the conjugate position of NLO chromophores for reducing the dipole moment and enhancing the electro-optic activities of organic materials  |  Zhang, H., Tian, Y., Bo, S., Xiao, L., Ao, Y., Zhang, J., & Li, M. 2020. ournal of Materials Chemistry C. 8(4): 1380-1390.
  12. First Report of Chenodeoxycholic Acid–Substituted Dyes Improving the Dye Monolayer Quality in Dye-Sensitized Solar Cells  |  Buene, A. F., Almenningen, D. M., Hagfeldt, A., Gautun, O. R., & Hoff, B. H. 2020. Solar Rrl. 4(4): 1900569.
  13. A review: methodologies for the synthesis of anthra [2, 3-b] thiophene and naphtho [2, 3-b: 6, 7-b'] dithiophene fragments for organic semiconductor materials  |  Mustafa, A., & Abid, M. A. 2022. Tetrahedron Letters. 113: 154258.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-Bromo-3-(bromomethyl)thiophene, 5 g

sc-254161
5 g
$183.00