Cas no 1480-87-1 (2-Fluoro-3-nitropyridine)

2-Fluoro-3-nitropyridine structure
2-Fluoro-3-nitropyridine structure
Product Name:2-Fluoro-3-nitropyridine
CAS No:1480-87-1
MF:C5H3FN2O2
MW:142.08792424202
MDL:MFCD03095068
CID:41449
PubChem ID:253661241
Update Time:2025-09-22

2-Fluoro-3-nitropyridine Chemical and Physical Properties

Names and Identifiers

    • 2-Fluoro-3-nitropyridine
    • 5-BroMo-2-fluoro-3-nitropyridine
    • 2-Fluor-3-nitropyridin
    • 2-fluoro-3-nitro-pyridine
    • 3-nitro-2-fluoropyridine
    • Pyridine,2-fluoro-3-nitro
    • 2-Fluoro-3-nitropyri
    • 2-Fluoro-3-nitrylpyridine
    • 3-bromo-2-fluoro-5-trifluoromethyl ryridine
    • 2-Fluoro-3-nitropyridine, 97+%
    • Pyridine, 2-fluoro-3-nitro-
    • PubChem1115
    • 2-fluor-3-nitropyridine
    • 2-fluoro-3- nitropyridine
    • KSC174G2N
    • QDKIYDGHCFZBGC-UHFFFAOYSA-N
    • BCP22086
    • SBB068995
    • 2-Fluoro-3-nitropyridine, AldrichCPR
    • VP10788
    • RP01306
    • AS04843
    • TRA0040046
    • LF10489
    • EN002078
    • SY019263
    • N390
    • FT-0650282
    • AM20070258
    • AC-6000
    • 1480-87-1
    • CS-D0967
    • AS-14963
    • F0982
    • A904181
    • SCHEMBL251800
    • EN300-41103
    • MFCD03095068
    • W-205674
    • AKOS005255936
    • DTXSID40376478
    • 2-Fluoro-3-nitropyridine,98%
    • DB-028058
    • MDL: MFCD03095068
    • Inchi: 1S/C5H3FN2O2/c6-5-4(8(9)10)2-1-3-7-5/h1-3H
    • InChI Key: QDKIYDGHCFZBGC-UHFFFAOYSA-N
    • SMILES: FC1C(=CC=CN=1)[N+](=O)[O-]

Computed Properties

  • Exact Mass: 142.01800
  • Monoisotopic Mass: 142.018
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 0
  • Complexity: 136
  • 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
  • Topological Polar Surface Area: 58.7
  • XLogP3: 1.1

Experimental Properties

  • Density: 1.439
  • Melting Point: 18°C(lit.)
  • Boiling Point: 110°C/10mmHg(lit.)
  • Flash Point: 103.842°C
  • Refractive Index: 1.5300 to 1.5340
  • Water Partition Coefficient: Slightly soluble in water.
  • PSA: 58.71000
  • LogP: 1.65210

2-Fluoro-3-nitropyridine Security Information

2-Fluoro-3-nitropyridine Customs Data

  • HS CODE:2933399090
  • Customs Data:

    China Customs Code:

    2933399090

    Overview:

    2933399090. Other compounds with non fused pyridine rings in structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

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2-Fluoro-3-nitropyridine Related Literature

  • 1. Nitro-heteroaromatic derivatives of amino-acids and peptides. Part IV. A circular dichroic method for the selective determination of cysteinyl residues
    C. Toniolo,D. Nisato,L. Biondi,A. Signor J. Chem. Soc. Perkin Trans. 1 1972 1182
  • 2. Nucleophilic displacement reactions in aromatic systems. Part X. Kinetics of the reactions of substituted α-halogenopyridines with aniline, N-methyl-, and N-ethyl-aniline in ethanol or ethyl acetate, and of 1-fluoro-2,4-dinitrobenzene with aniline in various solvents. The influence of basic catalysts
    Derek M. Brewis,Norman B. Chapman,John S. Paine,John Shorter,David J. Wright J. Chem. Soc. Perkin Trans. 2 1974 1787
  • 3. Methods of peptide sequencing. Part II. Cyclisation of N-2-amino-6-ntirophenyl and N-3-amino-2-pyridyl derivatives of amino-acids and peptides
    Robert A. W. Johnstone,T. Jeffrey Povall,Ian D. Entwistle J. Chem. Soc. Perkin Trans. 1 1975 1424
  • 4. Nitro-heteroaromatic derivatives of amino-acids and peptides. Part III. Application of ultraviolet–visible absorption and circular dichroism to N-(3-nitro-2-pyridyl)amino-acids
    C. Toniolo,D. Nisato,L. Biondi,A. Signor J. Chem. Soc. Perkin Trans. 1 1972 1179
  • 5. Nitro-heteroaromatic derivatives of amino-acids and peptides. Part V. Photochemical formation of 2-isobutylpyrido[2,3-d]imidazole 1-oxide from 3-nitro-2-pyridyl-DL-leucine
    G. G. Aloisi,E. Bordignon,A. Signor J. Chem. Soc. Perkin Trans. 2 1972 2218
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