6-FLUORO-5-NITRO-1H-INDAZOLE
- Product Name
- 6-FLUORO-5-NITRO-1H-INDAZOLE
- CAS No.
- 633327-51-2
- Chemical Name
- 6-FLUORO-5-NITRO-1H-INDAZOLE
- Synonyms
- 6-Fluoro-5-nitroindazole;6-FLUORO-5-NITRO-1H-INDAZOLE;5-nitro-6-fluoro-1H-indazole;1H-Indazole, 6-fluoro-5-nitro-
- CBNumber
- CB72449378
- Molecular Formula
- C7H4FN3O2
- Formula Weight
- 181.12
- MOL File
- 633327-51-2.mol
6-FLUORO-5-NITRO-1H-INDAZOLE Property
- Boiling point:
- 401.2±25.0 °C(Predicted)
- Density
- 1.629±0.06 g/cm3(Predicted)
- storage temp.
- Storage temp. 2-8°C
- pka
- 10.92±0.40(Predicted)
- Appearance
- Yellow to orange Solid
Safety
- HS Code
- 2933998090
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P271Use only outdoors or in a well-ventilated area.
P280Wear protective gloves/protective clothing/eye protection/face protection.
N-Bromosuccinimide Price
- Product number
- B440955
- Product name
- 6-fluoro-5-nitro-1H-indazole
- Packaging
- 10mg
- Price
- $45
- Updated
- 2021/12/16
- Product number
- HCH0353403
- Product name
- 6-FLUORO-5-NITRO-1H-INDAZOLE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $499.29
- Updated
- 2021/12/16
- Product number
- 35541
- Product name
- 6-Fluoro-5-nitro-1H-indazole
- Purity
- 95%
- Packaging
- 1g
- Price
- $700
- Updated
- 2021/12/16
- Product number
- 126237
- Product name
- 6-Fluoro-5-nitro-1H-indazole
- Purity
- >95%
- Packaging
- 1g
- Price
- $720
- Updated
- 2021/12/16
- Product number
- 633327512
- Product name
- 6-Fluoro-5-nitro-1H-indazole
- Packaging
- 5g
- Price
- $1100
- Updated
- 2021/12/16
6-FLUORO-5-NITRO-1H-INDAZOLE Chemical Properties,Usage,Production
Synthesis
348-25-4
633327-51-2
6-Fluoro-1H-indazole (1 g, 6.74 mmol) was used as a raw material and mixed with concentrated sulfuric acid. Concentrated sulfuric acid (22 mL) and potassium nitrate (0.74 g, 7.34 mmol) were added in batches at 0°C. After addition, stirring was continued for 10 minutes at room temperature. Upon completion of the reaction, the reaction mixture was cooled to 0 °C, alkalized to pH neutral with saturated sodium bicarbonate solution and subsequently extracted with ethyl acetate. The organic phase was washed with saturated brine and dried over anhydrous sodium sulfate. After concentration under reduced pressure to remove the solvent, the crude product was purified by fast column chromatography (eluent: dichloromethane/methanol=9.8:0.2) to afford 6-fluoro-5-nitro-1H-indazole (0.4 g, 30% yield) as a yellow solid.1H NMR (400 MHz, DMSO-d6) δ: 13.7 (broad peak, 1H), 8.78 (d, J=7.4 Hz, 1H ), 8.34 (s, 1H), 7.68 (d, J=11.8Hz, 1H). Mass spectrum (ESI) m/z: 180 ([M-H]-).
References
[1] Patent: WO2015/104662, 2015, A1. Location in patent: Page/Page column 38
[2] Patent: US2016/326151, 2016, A1. Location in patent: Paragraph 0208
[3] Bioorganic and Medicinal Chemistry, 2004, vol. 12, # 9, p. 2115 - 2137
6-FLUORO-5-NITRO-1H-INDAZOLE Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from 6-FLUORO-5-NITRO-1H-INDAZOLE manufacturers
- Product
- 6-Fluoro-5-nitro-1H-indazole 633327-51-2
- Price
- US $0.00-0.00/kg
- Min. Order
- 1kg
- Purity
- 98%
- Supply Ability
- kgs
- Release date
- 2023-01-03