ChemicalBook--->CAS DataBase List--->5228-49-9

5228-49-9

5228-49-9 Structure

5228-49-9 Structure
IdentificationMore
[Name]

1-METHYL-5-NITRO-1H-INDAZOLE
[CAS]

5228-49-9
[Synonyms]

1-METHYL-5-NITRO-1H-INDAZOLE
1-METHYL-5-NITROINDAZOLE
1-METHYL-5-NITRO-1H-INDAZOLE, 98+%
[EINECS(EC#)]

-0
[Molecular Formula]

C8H7N3O2
[MDL Number]

MFCD01318163
[Molecular Weight]

177.16
[MOL File]

5228-49-9.mol
Chemical PropertiesBack Directory
[Melting point ]

161-162°C
[Boiling point ]

332.9±15.0 °C(Predicted)
[density ]

1.42±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

solid
[pka]

-0.82±0.30(Predicted)
[color ]

yellow
[BRN ]

168080
[CAS DataBase Reference]

5228-49-9(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R20/22:Harmful by inhalation and if swallowed .
R68:Possible risk of irreversible effects.
[Safety Statements ]

S22:Do not breathe dust .
S36/37:Wear suitable protective clothing and gloves .
[RIDADR ]

2811
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[PackingGroup ]

II
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

1-METHYL-5-NITRO-1H-INDAZOLE(5228-49-9)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

1-Methyl-5-nitro-1H-indazole, 98+%(5228-49-9)
Hazard InformationBack Directory
[Synthesis]

5-Nitroindazole

5401-94-5

Iodomethane

74-88-4

2-METHYL-5-NITRO-2H-INDAZOLE

5228-48-8

1-METHYL-5-NITRO-1H-INDAZOLE

5228-49-9

GENERAL METHOD: Cesium carbonate (12.26 mmol) was added to a solution of 5-nitroindazole (6.13 mmol) in tetrahydrofuran (THF; 25 mL) at 0 °C. The reaction mixture was stirred at 0 °C for 15 min before iodomethane or allyl bromide (6.13 mmol) was added dropwise. The progress of the reaction was monitored by thin layer chromatography (TLC) until the starting material completely disappeared. After completion of the reaction, the mixture was concentrated. The crude product was dissolved in ethyl acetate (EtOAc; 50 mL), washed sequentially with water and brine, and the organic phase was dried over anhydrous magnesium sulfate (MgSO?). The solvent was removed by evaporation under reduced pressure, and the resulting residue was purified by silica gel column chromatography with ethyl acetate/hexane (3:7, v/v) as eluent to afford 1-alkyl-5-nitroindazole and 2-alkyl-5-nitroindazole, respectively.

[References]

[1] Synthetic Communications, 2015, vol. 45, # 17, p. 2005 - 2013
[2] Tetrahedron, 2008, vol. 64, # 28, p. 6711 - 6723
[3] Patent: US2014/371219, 2014, A1. Location in patent: Paragraph 0659; 0660; 0661
[4] Patent: WO2016/57834, 2016, A1. Location in patent: Paragraph 000406
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