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Detail of "1682-20-8"

  • MSDS Download
  • CAS Number:
  • 1682-20-8
  • Name:
  • 4-Amino-2,3,5,6-tetrafluoropyridine

  • Molecular Structure:
  • Formula:
  • C5H2F4N2
  • Molecular Weight:
  • 166.08
  • Synonyms:
  • 2,3,5,6-tetrafluoropyridin-4-amine;2,3,5,6-tetrafluoro-pyridin-4-ylamine;
  • Density:
  • 1.631g/cm3
  • Melting Point:
  • 85-87 °C(lit.)
  • Boiling Point:
  • 208.3°Cat760mmHg
  • Flash Point:
  • 79.8°C
  • Hazard Symbols:
  • Risk Codes:
  • R20/21/22;R36/37/38   
  • Safety:
  • Hazard Codes Xn,Xi
    Risk Statements 20/21/22-36/37/38
    Safety Statements 26-36
    WGK Germany 3
    Hazard Note Irritant
    Details

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CAS No.1682-20-8 4-Amino-2,3,5,6-tetrafluoropyridine

4-Amino-2,3,5,6-tetrafluoropyridine

Supplier:Shanghai Sinofluoro Scientific Co., Ltd [ China (Mainland)]

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CAS No.1682-20-8 4-Amino-2,3,5,6-tetrafluoropyridine

4-Amino-2,3,5,6-tetrafluoropyridine

Supplier:Agno Pharma [ United States]

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Address:683 N. Mountain Road,Newington,CT,6111,USA

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CAS No.1682-20-8 4-Amino-2,3,5,6-tetrafluoropyridine

Supplier:Nanjing Lynsci Chemical Co., Ltd [ China (Mainland)]

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CAS No.1682-20-8 4-Amino-2,3,5,6-tetrafluoropyridine

Supplier:Beijing zhongke expanding chemical technology Co., LTD. [ China (Mainland)]

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CAS No.1682-20-8 4-Amino-2,3,5,6-tetrafluoropyridine

Supplier:Shanghai Fchemicals Technology Co., Ltd [ China (Mainland)]

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CAS No.1682-20-8 4-Amino-2,3,5,6-tetrafluoropyridine

Supplier:Bernhagen-Chemie GmbH [ Germany]

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Reference

4-Amino-3-halo-2-pyridinone nucleoside and nucleotide compounds as antiviral and antitumor agents
4-Amino-3-halo-2-pyridinone nucleoside and nucleotide compounds as antiviral and antitumor agents. McNamara, Dennis J.; Cook, Phillip Dan (Warner-Lambert Co., USA). Eur. Pat. Appl. EP 210639 A2 4 Feb 1987, 15 pp. DESIGNATED STATES: R: AT, BE, CH, DE, FR, GB, IT, LI, LU, NL, SE. (European Patent Organization) CODEN: EPXXDW. CLASS: ICM: C07H019-048. ICS: A61K031-70. APPLICATION: EP 86-110427 29 Jul 1986. PRIORITY: US 85-759816 29 Jul 1985. DOCUMENT TYPE: Patent CA Section: 33 (Carbohydrates) Section cross-reference(s): 1 The title compds. [I; R1 = F, Cl, Br; R2 = H, OH, F, BzO, 4-MeC6H4CO2, alkanoyloxy; R3 = H, F; R4 = OH, BzO, 4-MeC6H4CO2, alkanoyloxy; R5 = (HO)2P(O)O, R4] were prepd. as virucides and neoplasm inhibitors. Pentafluoropyridine was treated successively with aq. NH3, 1M NaOH, and defluorinated with anhyd. hydrazine to give 4-amino-3-fluoro-2(1H)pyridinone. This was treated successively with (Me3Si)2NH and 1-O-acetyl-2,3,5-tri-O-benzoyl-b-D-ribofuranose/SnCl4 to give I (R1 = F, R2 = R4 = R5 = BzO, R3 = H) which was treated with NaOMe in MeOH to give ribofuranosylpyridinone II. 1682-20-8 and 107842-72-8 which are cas registry numbers of substances are two of reagents here. II had VR values of 1.10 against rhino-2 virus and 1.41 against vaccinia virus. .
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