Date published: 2026-4-19

1-800-457-3801

SCBT Portrait Logo
Seach Input

9-(2,2-Dicyanovinyl)julolidine (CAS 58293-56-4)

5.0(1)
Write a reviewAsk a question

Alternate Names:
9-Julolidinylmethylenemalononitrile; DCVJ
Application:
9-(2,2-Dicyanovinyl)julolidine is a fluorescent probe used for binding to proteins etc
CAS Number:
58293-56-4
Molecular Weight:
249.31
Molecular Formula:
C16H15N3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

9-(2,2-Dicyanovinyl)julolidine, referred to as DCVJ, is a synthetic organic compound extensively employed in diverse scientific research endeavors. This highly reactive and versatile molecule serves as an optimal choice for a wide spectrum of laboratory experiments. It exhibits solubility in water, alcohol, and ether. The applications of 9-(2,2-Dicyanovinyl)julolidine in scientific research span a broad range. It serves as a valuable reagent in organic synthesis, a catalyst in polymerization reactions, and a solvent in the preparation of polymers and various materials. Functioning as a nucleophile, 9-(2,2-Dicyanovinyl)julolidine possesses the capability to form covalent bonds with electron-deficient species. This reaction occurs when the nucleophile attacks the electron-deficient species, such as an alkene or carbonyl group, resulting in the establishment of a new covalent bond. This particular reaction, known as an addition reaction, serves as the foundation for various synthetic organic reactions.


9-(2,2-Dicyanovinyl)julolidine (CAS 58293-56-4) References

  1. Fluorescence anisotropy of molecular rotors.  |  Levitt, JA., et al. 2011. Chemphyschem. 12: 662-72. PMID: 21328515
  2. Intrinsic and extrinsic temperature-dependency of viscosity-sensitive fluorescent molecular rotors.  |  Howell, S., et al. 2012. J Fluoresc. 22: 457-65. PMID: 21947609
  3. A Flow-Cytometry-Based Approach to Facilitate Quantification, Size Estimation and Characterization of Sub-visible Particles in Protein Solutions.  |  Lubich, C., et al. 2015. Pharm Res. 32: 2863-76. PMID: 25788448
  4. No Touching! Abrasion of Adsorbed Protein Is the Root Cause of Subvisible Particle Formation During Stirring.  |  Sediq, AS., et al. 2016. J Pharm Sci. 105: 519-529. PMID: 26869415
  5. Fluorescence Turn-On Sensing of DNA Duplex Formation by a Tricyclic Cytidine Analogue.  |  Burns, DD., et al. 2017. J Am Chem Soc. 139: 1372-1375. PMID: 28080035
  6. Stimulation of synaptoneurosome glutamate release by monomeric and fibrillated α-synuclein.  |  Sarafian, TA., et al. 2017. J Neurosci Res. 95: 1871-1887. PMID: 28117497
  7. Flow-dependent fluorescence of CCVJ.  |  Schmidt, MJ., et al. 2017. J Biol Eng. 11: 24. PMID: 28785307
  8. Electrostatic lipid-protein interactions sequester the curli amyloid fold on the lipopolysaccharide membrane surface.  |  Swasthi, HM. and Mukhopadhyay, S. 2017. J Biol Chem. 292: 19861-19872. PMID: 29021250
  9. Compositional adaptability in NPM1-SURF6 scaffolding networks enabled by dynamic switching of phase separation mechanisms.  |  Ferrolino, MC., et al. 2018. Nat Commun. 9: 5064. PMID: 30498217
  10. Cholesterol-Based Compounds: Recent Advances in Synthesis and Applications.  |  Albuquerque, HMT., et al. 2018. Molecules. 24: PMID: 30597999
  11. A Method for High-Throughput Measurements of Viscosity in Sub-micrometer-Sized Membrane Systems.  |  Chwastek, G., et al. 2020. Chembiochem. 21: 836-844. PMID: 31566864
  12. Detection and Quantification of Nonlabeled Polystyrene Nanoparticles Using a Fluorescent Molecular Rotor.  |  Moraz, A. and Breider, F. 2021. Anal Chem. 93: 14976-14984. PMID: 34735123
  13. Isolation and Quantification of Polystyrene Nanoplastics in Tissues by Low Pressure Size Exclusion Chromatography.  |  Gagné, F. 2022. J Xenobiot. 12: 109-121. PMID: 35645291

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

9-(2,2-Dicyanovinyl)julolidine, 5 mg

sc-210694
5 mg
$52.00