| Identification | Back Directory | [Name]
(4-NITRO-PYRAZOL-1-YL)-ACETIC ACID | [CAS]
6645-69-8 | [Synonyms]
AKOS B000219 AKOS PAO-0916 ART-CHEM-BB B000219 CHEMBRDG-BB 5913009 TIMTEC-BB SBB000166 2-(4-nitro-1-pyrazolyl)acetic acid 2-(4-nitropyrazol-1-yl)acetic acid (4-NITRO-PYRAZOL-1-YL)-ACETIC ACID 1H-Pyrazole-1-acetic acid, 4-nitro- (4-NITRO-1H-PYRAZOL-1-YL)ACETIC ACID 2-(4-nitropyrazol-1-yl)ethanoic acid 2-(4-NITRO-1H-PYRAZOL-1-YL)ACETIC ACID (4-nitro-1H-pyrazol-1-yl)acetic acid(SALTDATA: FREE) | [Molecular Formula]
C5H5N3O4 | [MDL Number]
MFCD00296933 | [MOL File]
6645-69-8.mol | [Molecular Weight]
171.11 |
| Chemical Properties | Back Directory | [Boiling point ]
416.4±25.0 °C(Predicted) | [density ]
1.71±0.1 g/cm3(Predicted) | [storage temp. ]
2-8°C | [pka]
3.33±0.10(Predicted) | [Appearance]
White to light yellow Solid |
| Hazard Information | Back Directory | [Uses]
(4-Nitro-1H-pyrazol-1-yl)acetic Acid is used in pharmacological study of effects of C-nitropyrazoles and C-nitroazoles on ocular blood flow and retinal function recovery after ischemic insult. | [Synthesis]
An aqueous solution (100 mL) of potassium hydroxide (32.7 g, 0.58 mol) was slowly added to an acetone solution (500 mL) of 4-nitro-1H-pyrazole (30 g, 0.27 mol) under stirring at room temperature. After 30 minutes of reaction, an acetone solution (100 mL) of 2-bromoacetic acid (38.7 g, 0.27 mol) was added dropwise. The reaction mixture was continued to be stirred overnight. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was diluted with water and extracted three times with ethyl acetate, the organic phases were combined and concentrated under reduced pressure. Subsequently, the residue was further extracted with a solvent mixture of dichloromethane and methanol, and the organic phases were combined and concentrated again under reduced pressure to give the target product 2-(4-nitro-1H-pyrazol-1-yl)acetic acid (40 g, 88% yield). | [References]
[1] Patent: WO2013/174895, 2013, A1. Location in patent: Page/Page column 70 |
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Biokitchen
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021-021-021-31663258 13795219287 |
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Wuxi AppTec
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022-59987777 13552403979 |
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www.labnetwork.com |
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Energy Chemical
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http://www.energy-chemical.com |
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