ChemicalBook--->CAS DataBase List--->25391-58-6

25391-58-6

25391-58-6 Structure

25391-58-6 Structure
IdentificationBack Directory
[Name]

2-HYDROXY-3-IODO-5-NITROPYRIDINE 97
[CAS]

25391-58-6
[Synonyms]

3-IODO-5-NITROPYRIDIN-2-OL
3-iodo-5-nitropyridin-2(1H)-one
2(1H)-Pyridinone, 3-iodo-5-nitro-
2-HYDROXY-3-IODO-5-NITROPYRIDINE 97
3-iodo-5-nitro-1,2-dihydropyridin-2-one
2-Hydroxy-3-iodo-5-nitropyridine≥ 99% (HPLC)
2-HYDROXY-3-IODO-5-NITROPYRIDINE 97 ISO 9001:2015 REACH
[Molecular Formula]

C5H3IN2O3
[MDL Number]

MFCD06008303
[MOL File]

25391-58-6.mol
[Molecular Weight]

265.99
Chemical PropertiesBack Directory
[Melting point ]

203-207 °C(lit.)
[Boiling point ]

317.9±42.0 °C(Predicted)
[density ]

2.27±0.1 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[form ]

solid
[pka]

6.62±0.10(Predicted)
[Appearance]

Light yellow to yellow Solid
[InChI]

1S/C5H3IN2O3/c6-4-1-3(8(10)11)2-7-5(4)9/h1-2H,(H,7,9)
[InChIKey]

DPHDSYLWPVMRTM-UHFFFAOYSA-N
[SMILES]

Oc1ncc(cc1I)[N+]([O-])=O
Safety DataBack Directory
[Symbol(GHS) ]


GHS05,GHS07
[Signal word ]

Danger
[Hazard statements ]

H302-H318
[Precautionary statements ]

P280-P301+P312+P330-P305+P351+P338+P310
[Hazard Codes ]

Xn
[Risk Statements ]

22-41
[Safety Statements ]

26-39
[WGK Germany ]

3
[HS Code ]

2933399990
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Dam. 1
Hazard InformationBack Directory
[Chemical Properties]

Brick red to brown powder
[Synthesis]

2-Hydroxy-5-nitropyridine

5418-51-9

2-HYDROXY-3-IODO-5-NITROPYRIDINE  97

25391-58-6

Synthesis of 3-iodo-5-nitropyridin-2-ol (CXXI): a mixture of 2-hydroxy-5-nitropyridine (14 g, 99.9 mmol) and potassium carbonate (13.8 g, 99.9 mmol) was dissolved in N,N-dimethylformamide (100 mL). Iodine (25.3 g, 99.7 mmol) was added in batches at room temperature. The reaction mixture was heated at 85 °C for 15 h and subsequently cooled to room temperature. The reaction process was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the mixture was diluted with water (150 mL) and extracted with ethyl acetate (75 mL x 3). The organic phases were combined, washed with brine (150 mL × 3), dried over anhydrous sodium sulfate, and subsequently concentrated in vacuum. The residual solid was washed with hexane (50 mL × 2) and dried under a stream of air to afford the brown solid CXXI (14 g, 53% yield), which could be used in subsequent reactions without further purification.

[References]

[1] Australian Journal of Chemistry, 2008, vol. 61, # 6, p. 438 - 445
[2] Patent: WO2015/73528, 2015, A1. Location in patent: Page/Page column 191
[3] Journal of Medicinal Chemistry, 2002, vol. 45, # 13, p. 2841 - 2849
[4] Fortschr. Teerfarbenfabr. Verw. Industriezweige, 1930, vol. 17, p. 2439
[5] Patent: US1753170, 1926,
Spectrum DetailBack Directory
[Spectrum Detail]

2-HYDROXY-3-IODO-5-NITROPYRIDINE 97(25391-58-6)1HNMR
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