(1,2-DIBROMOETHYL)BENZENE (CAS 93-52-7)
(1,2-DIBROMOETHYL)BENZENE (CAS:
93-52-7) has molecular formula C8H8Br2 and molecular weight 263.96 g/mol. This compound has been the subject of numerous scientific investigations due to its structural features and practical utility in synthetic chemistry and industrial processes. View product details →
Product Background
This comprehensive research profile examines the scientific literature surrounding (1,2-DIBROMOETHYL)BENZENE.
Key Research Findings
- Recent detections of benzonitrile and other aromatic compounds in interstellar clouds and comets have revealed a rich aromatic astrochemistry.
- Our results show the appearance of a spectrum and wave amplitudes reminiscent of that of benzene.
- On subjecting the benzene molecule to a linear applied field, the resulting field-modified site energies are obtained, by projecting the site-energy locations onto a corresponding
- Invoking the Lippmann-Schwinger scattering theory enables the spectral energy transmission function T to be found for each of the benzene types.
Detailed Literature Analysis
Below are the top-ranked research papers for (1,2-DIBROMOETHYL)BENZENE, presented with bibliographic details and scientific abstracts.
Synthetic Chemistry
1. Enhancing the Photocatalytic Performance of CsPbBr
Excited-state interactions at the interfaces of nanocrystals play a crucial role in determining photocatalytic efficiency. CsPbBr
Biological & Pharmacological Studies
2. Characterization of monosubstituted benzene ices
Aromatic structures are fundamental for key biological molecules such as RNA and metabolites and the abundances of aromatic molecules on young planets are therefore of high interest. Recent detections of benzonitrile and other aromatic compounds in interstellar clouds and comets have revealed a rich aromatic astrochemistry. In the cold phases of st
3. Molecular orbitals of an elastic artificial benzene
Benzene, a hexagonal molecule with formula CH, is one of the most important aromatic hydrocarbons. Its structure arises from the hybridization from which three in-plane -bonds are formed. A fourth -orbital perpendicular to the molecular plane combines with those arising from other carbon atoms to form -bonds, very important to describe the electron
Other Research
4. Applied-Field Effects on Benzene Transmission
By expressing the discrete Schrodinger equation as a second-order finite-difference equation with constant coefficients, the renormalization equations for substituted benzene dimers are derived via the c_n-coefficient elimination procedure. On subjecting the benzene molecule to a linear applied field, the resulting field-modified site energies are
5. Overlap Effects on Benzene Transmission
The Huckel molecular-orbital method (with overlap S) is used to derive the S-modified version of the renormalization equations, which are then employed to introduce overlap into the para-, meta- and ortho-benzene dimers' parameters. Invoking the Lippmann-Schwinger scattering theory enables the spectral energy transmission function T(E) to be found
6. A benzene interference single-electron transistor
Interference effects strongly affect the transport characteristics of a benzene single-electron transistor (SET) and for this reason we call it interference SET (I-SET). We focus on the effects of degeneracies between many-body states of the isolated benzene. We show that the particular current blocking and selective conductance suppression occurri
Conclusion
The research literature on (1,2-DIBROMOETHYL)BENZENE demonstrates sustained scientific interest, with publications continuing through 0. The compound serves as an important building block in synthetic chemistry and has been explored for various applications. Researchers and industrial users can view detailed specifications or submit an inquiry for pricing and availability.
Data Sources: PubMed/MEDLINE, CrossRef. 6 papers analyzed. Last updated: 2026-05-25. This article is automatically generated from peer-reviewed research data.