Cas no 2486-04-6 (2,4-Dinitrobiphenyl)

2,4-Dinitrobiphenyl structure
2,4-Dinitrobiphenyl structure
Product Name:2,4-Dinitrobiphenyl
CAS No:2486-04-6
MF:C12H8N2O4
MW:244.202922821045
CID:288326
PubChem ID:94927
Update Time:2025-04-19

2,4-Dinitrobiphenyl Chemical and Physical Properties

Names and Identifiers

    • 2,4-Dinitrobiphenyl
    • 2,4-Dinitrobiphenyl; 2,4-dinitrobiphenyl; 2,4-dinitro-biphenyl; CCRIS 4053; AC1L3T79; NSC8739; 2,4-DINITRODIPHENYL; AC1Q20S9; CTK1A7347; o,p-Dinitrodiphenyl; 2.4-Dinitro-biphenyl;
    • 2,4-DINITRODIPHENYL
    • NSC-8739
    • CCRIS 4053
    • 1,1'-Biphenyl, 2,4-dinitro-
    • 2486-04-6
    • NSC8739
    • JLV8PZV32V
    • DTXSID10179559
    • SCHEMBL2137404
    • NSC 8739
    • 2,4-dinitro-1,1'-biphenyl
    • Inchi: 1S/C12H8N2O4/c15-13(16)10-6-7-11(12(8-10)14(17)18)9-4-2-1-3-5-9/h1-8H
    • InChI Key: DBTRHJMMJLOORC-UHFFFAOYSA-N
    • SMILES: [O-][N+](C1C=C(C=CC=1C1C=CC=CC=1)[N+](=O)[O-])=O

Computed Properties

  • Exact Mass: 244.04844
  • Monoisotopic Mass: 244.04840674g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 1
  • Complexity: 317
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 3.2
  • Topological Polar Surface Area: 91.6?2

Experimental Properties

  • PSA: 86.28
  • LogP: 4.21640

2,4-Dinitrobiphenyl Related Literature

  • 1. 117. The ullman biaryl synthesis. Part I. Atypical products of syntheses of 2,4-dinitrobiphenyl and related compounds
  • 2. 122. The Ullmann biaryl synthesis. Part VI. The scope and mechanism of the reaction
  • 3. 883. A novel intramolecular nucleophilic displacement
    D. H. Hey,J. A. Leonard,C. W. Rees J. Chem. Soc. 1962 4579
  • 4. 311. The nitration of p-terphenyl in glacial acetic acid
    P. Culling,G. W. Gray,D. Lewis J. Chem. Soc. 1960 1547
  • 5. 120. The Ullmann biaryl synthesis. Part IV. The halogen-transfer
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