Date published: 2025-12-6

1-800-457-3801

SCBT Portrait Logo
Seach Input

trans-1,4-Dibromo-2-butene (CAS 821-06-7)

0.0(0)
Write a reviewAsk a question

CAS Number:
821-06-7
Molecular Weight:
213.90
Molecular Formula:
C4H6Br2
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.

QUICK LINKS

trans-1,4-Dibromo-2-butene is used as a reagent in the preparation of diaminoalkenes though copper-mediated diamination reaction. It is used as a monomer to create polymers such as cationic polymerization or benzalkonium chloride. trans-1,4-Dibromo-2-butene also has antimicrobial properties and may act to inhibit the activity of bacteria by blocking protein synthesis and cell division. Additionally, it is used for the synthesis of a other organic compounds, such as polymers, dyes, more.


trans-1,4-Dibromo-2-butene (CAS 821-06-7) References

  1. Medicinal chemistry of Annonaceous acetogenins: design, synthesis, and biological evaluation of novel analogues.  |  Kojima, N. and Tanaka, T. 2009. Molecules. 14: 3621-61. PMID: 19783948
  2. Synthesis, fluorine-18 radiolabeling, and biological evaluation of N-((E)-4-fluorobut-2-en-1-yl)-2beta-carbomethoxy-3beta-(4'-halophenyl)nortropanes: candidate radioligands for in vivo imaging of the brain dopamine transporter with positron emission tomography.  |  Stehouwer, JS., et al. 2010. J Med Chem. 53: 5549-57. PMID: 20597489
  3. Synthesis and pharmacological evaluation of fluorine-containing D₃ dopamine receptor ligands.  |  Tu, Z., et al. 2011. J Med Chem. 54: 1555-64. PMID: 21348515
  4. Preparation of 1-Tosyloxy-4-Substituted-2-butenes Using Ag(I) Salts.  |  Stehouwer, JS. and Goodman, MM. 2015. Tetrahedron Lett. 56: 4480-4482. PMID: 26309335
  5. Conformational Restriction of Peptides Using Dithiol Bis-Alkylation.  |  Peraro, L., et al. 2016. Methods Enzymol. 580: 303-32. PMID: 27586339
  6. Cross-Linking of a Hydrophilic, Antimicrobial Polycation toward a Fast-Swelling, Antimicrobial Superabsorber and Interpenetrating Hydrogel Networks with Long Lasting Antimicrobial Properties.  |  Strassburg, A., et al. 2017. ACS Appl Mater Interfaces. 9: 36573-36582. PMID: 28952307
  7. Synthesis and Properties of Side-Chain Functionalized Polytetrahydrofuran Derivatives via the Blue-Light Photocatalytic Thiol-Ene Reaction.  |  Zhu, X., et al. 2019. Polymers (Basel). 11: PMID: 30960567
  8. Characterization and Optimization of PLA Stereocomplexed Hydrogels for Local Gene Delivery Systems.  |  Liu, KY., et al. 2019. Polymers (Basel). 11: PMID: 31058859
  9. Synthesis, Structure, and Reactivity of Binaphthyl Supported Dihydro[1,6]diazecines.  |  Lemmerer, M., et al. 2019. Molecules. 24: PMID: 31455006
  10. Naphthalene-Diimide-Based Ionenes as Universal Interlayers for Efficient Organic Solar Cells.  |  Liu, M., et al. 2020. Angew Chem Int Ed Engl. 59: 18131-18135. PMID: 32558039
  11. A cell permeable bimane-constrained PCNA-interacting peptide.  |  Horsfall, AJ., et al. 2021. RSC Chem Biol. 2: 1499-1508. PMID: 34704055
  12. Surface and thermal properties of synthesized cationic poly(ethylene oxide) gemini surfactants: the role of the spacer.  |  Hussain, SMS., et al. 2019. RSC Adv. 9: 30154-30163. PMID: 35530216
  13. Oligonucleotide nanoassemblies with allyl bromide scaffold-based small molecules.  |  Abbas, SJ., et al. 2023. Discov Nano. 18: 81. PMID: 37382753

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

trans-1,4-Dibromo-2-butene, 1 g

sc-255668A
1 g
$30.00

trans-1,4-Dibromo-2-butene, 5 g

sc-255668B
5 g
$43.00

trans-1,4-Dibromo-2-butene, 25 g

sc-255668
25 g
$87.00

trans-1,4-Dibromo-2-butene, 100 g

sc-255668C
100 g
$286.00