Skip to content
DraconiticResearch
Search Sources API
203,952 studies31 sourcesUpdated 23 min ago
Peer-reviewedCC BYIUCrData

6,7-Di-bromo-2-methyl-3-phenyl-quinoxaline.

  1. 1Department of Chemistry & Biochemistry Central Connecticut State University, 1619 Stanley Street New Britain CT 06053 USA.
  2. 2The University of Edinburgh School of Chemistry Joseph Black Building David Brewster Road Edinburgh EH9 3FJ United Kingdom.

Abstract

The title com-pound, C15H10Br2N2, was synthesized using the acid catalyst NH4HF2 in a water/methanol solution. There are two mol-ecules per asymmetric unit where the quinoxaline moieties make dihedral angles of 48.05 (4) and 40.83 (5)° with respect to their phenyl rings. In the extended structure, mol-ecules form layers stacked along (001) that are held together by hy-dro-gen and halogen bonds.

Related

  1. Synthesis and structure of catena-poly[[[aquazinc(II)]-μ-2-({[amino­(sulfanid­yl)methyl­idene]amino}­imino)-2-phenyl­acetato-κ4O,N,S:O′] monohydrate]
    Javokhirkhon Akhatov, Gulnora Tillaeva, Khayit Turaev +4
    Acta Crystallographica Section E: Crystallographic CommunicationsPeer-reviewedCC BYFull textGeneral chemistryEurope PMC
  2. Crystal structure of 1-[(4-methyl-phen-yl)sulfon-yl]-2-phenyl-azetidine.
    Berthy J Aroche, Katherine Barraza Hernandez, Zoe Y Marr +2
    Acta crystallographica. Section E, Crystallographic communicationsPeer-reviewedCC BYFull textInorganic & organometallic chemistryEurope PMC
  3. Synthesis, crystal structure, Hirshfeld surface analysis and halogen-involving interactions in a bromo/chloro-substituted Schiff base 1-(3-bromo-4,5-dimethoxyphenyl)-N-(2,4-dichlorophenyl)methanimine
    Charef Tabti, Hafsa Khaldi, Abdelmadjid Benmohammed +4
    Acta Crystallographica Section C : Structural Chemistry [2014-...]Peer-reviewedPublisher termsFull textInorganic & organometallic chemistryOrganic chemistryHAL
  4. Quinoxaline-Triazole Hybrids: Exploring the Impact of Substituent Architecture on Cytotoxic Potency and Receptor Interaction.
    Bangar Reddy Vancha, Mandapalli Sreeshitha, Shaik Farheen Banu +7
    Chemistry & biodiversityPeer-reviewedCC BY-NCFull textOrganic chemistryEurope PMCPMC
  5. Preliminary in vitro evaluation of anti-leukemic and antimalarial activities of pyrrolo[1,2-a]quinoxaline-carboxylic acid hydrazone derivatives.
    Jean Gullion, Noël Pinaud, Lindita Lari +11
    Acta Chimica SlovenicaPeer-reviewedCC BY-SA 4.0Full textOrganic chemistryHAL
BibTeX
@article{valentin202667dibromo2methyl3phenylquinoxaline,
  title = {{6,7-Di-bromo-2-methyl-3-phenyl-quinoxaline.}},
  author = {Avion T Valentin and Guy Crundwell and Gary S Nichol},
  journal = {IUCrData},
  year = {2026},
  month = sep,
  doi = {10.1107/s2414314626010278},
  url = {https://europepmc.org/article/MED/42997249},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - 6,7-Di-bromo-2-methyl-3-phenyl-quinoxaline.
AU  - Avion T Valentin
AU  - Guy Crundwell
AU  - Gary S Nichol
PY  - 2026
DA  - 2026/09/01
JO  - IUCrData
DO  - 10.1107/s2414314626010278
UR  - https://europepmc.org/article/MED/42997249
AB  - The title com-pound, C15H10Br2N2, was synthesized using the acid catalyst NH4HF2 in a water/methanol solution. There are two mol-ecules per asymmetric unit where the quinoxaline moieties make dihedral angles of 48.05 (4) and 40.83 (5)° with respect to their phenyl rings. In the extended structure, mol-ecules form layers stacked along (001) that are held together by hy-dro-gen and halogen bonds.
SN  - 2414-3146
ER  -