ChemicalBook--->CAS DataBase List--->914311-50-5

914311-50-5

914311-50-5 Structure

914311-50-5 Structure
IdentificationBack Directory
[Name]

3-AMINO-4-BROMO-1H-INDAZOLE
[CAS]

914311-50-5
[Synonyms]

4-Bromo-1H-indazol-3-amine
4-bromo-2H-indazol-3-amine
3-AMINO-4-BROMO-1H-INDAZOLE
1H-Indazol-3-aMine, 4-broMo-
4-BroMo-1H-indazol-3-ylaMine
[Molecular Formula]

C7H6BrN3
[MDL Number]

MFCD09909580
[MOL File]

914311-50-5.mol
[Molecular Weight]

212.05
Chemical PropertiesBack Directory
[Melting point ]

142-144℃
[Boiling point ]

431.3±25.0 °C(Predicted)
[density ]

1.867±0.06 g/cm3(Predicted)
[storage temp. ]

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

Slightly soluble.
[form ]

Crystalline Powder
[pka]

13.68±0.40(Predicted)
[color ]

Off-white to brown to gray
Safety DataBack Directory
[Hazard Codes ]

T
[Risk Statements ]

25
[Safety Statements ]

45
[RIDADR ]

UN2811
[HazardClass ]

IRRITANT
[HS Code ]

29339980
Hazard InformationBack Directory
[Uses]

Microwave heating of 2-halobenzaldehydes or 2-haloacetophenones with phenylhydrazines at 160°C for 10 min quantitatively yielded the arylhydrazones, which were further cyclized to give 1-aryl-1H-indazoles via CuI/diamine-catalyzed N-arylation under microwave heating (160°C, 10 min). Good to excellent yields were observed for 2-iodo, 2-bromo, and 2-chloro benzaldehydes or acetophenones.
[Synthesis]

A solution of 2-fluoro-6-bromobenzonitrile (22.0 mmol) and 98% hydrazine hydrate (90.0 mmol) in n-butanol (15 ml) was stirred at reflux for 7 hours. The mixture was cooled to room temperature. The resulting mixture was concentrated under reduced pressure
Spectrum DetailBack Directory
[Spectrum Detail]

3-AMINO-4-BROMO-1H-INDAZOLE(914311-50-5)1HNMR
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