ISOXAZOLE, 4-NITRO-
- Product Name
- ISOXAZOLE, 4-NITRO-
- CAS No.
- 1121-13-7
- Chemical Name
- ISOXAZOLE, 4-NITRO-
- Synonyms
- 4-Nitroisoxazole;4-nitro-1,2-oxazole;ISOXAZOLE, 4-NITRO-
- CBNumber
- CB5840337
- Molecular Formula
- C3H2N2O3
- Formula Weight
- 114.06
- MOL File
- 1121-13-7.mol
ISOXAZOLE, 4-NITRO- Property
- Melting point:
- 46-47 °C
- Boiling point:
- 243.5±13.0 °C(Predicted)
- Density
- 1.475±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- pka
- -5.58±0.50(Predicted)
- Appearance
- Light brown to brown Solid
Safety
- HS Code
- 2934999090
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H332Harmful if inhaled
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- N901073
- Product name
- 4-Nitroisoxazole
- Packaging
- 10mg
- Price
- $45
- Updated
- 2021/12/16
- Product number
- X8994
- Product name
- 4-Nitroisoxazole
- Packaging
- 250mg
- Price
- $188
- Updated
- 2021/12/16
- Product number
- OR904227
- Product name
- 4-Nitroisoxazole
- Purity
- 96%
- Packaging
- 1g
- Price
- $327
- Updated
- 2021/12/16
- Product number
- X8994
- Product name
- 4-Nitroisoxazole
- Packaging
- 1g
- Price
- $355
- Updated
- 2021/12/16
- Product number
- 072478
- Product name
- 4-Nitroisoxazole
- Purity
- 95+%
- Packaging
- 250mg
- Price
- $416
- Updated
- 2021/12/16
ISOXAZOLE, 4-NITRO- Chemical Properties,Usage,Production
Synthesis
288-14-2
1121-13-7
General procedure for the synthesis of 4-nitroisoxazole from isoxazole: ammonium nitrate (1.8 g, 22.5 mmol) was added to a solution of trifluoroacetic anhydride (7 mL, 50.7 mmol) of isoxazole (1 g, 14.5 mmol) in batches of 0.3 g each, and the temperature of the reaction was controlled to be between 25 and 30 °C. After the addition was completed, the reaction mixture was slowly poured into ice water and extracted with dichloromethane (15 mL x 4). The organic phases were combined, washed with water and the aqueous layer was then extracted with dichloromethane. The combined dichloromethane extracts were dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give a yellow-green oil. The oily material was ground with hexane under the condition of cooling to 50 ℃, a solid was precipitated, and 4-nitroisoxazole was obtained by filtration (0.72 g, 44% yield).
References
[1] Journal of Organic Chemistry, 1987, vol. 52, # 13, p. 2714 - 2726
[2] Helvetica Chimica Acta, 1989, vol. 72, p. 556 - 569
[3] Patent: WO2009/154769, 2009, A1. Location in patent: Page/Page column 37-38
[4] Zhurnal Obshchei Khimii, 1959, vol. 29, p. 535,538; engl. Ausg. S. 533
[5] Patent: WO2011/38572, 2011, A1. Location in patent: Page/Page column 76
ISOXAZOLE, 4-NITRO- Preparation Products And Raw materials
Raw materials
Preparation Products
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