| Identification | More | [Name]
5-Hydroxy-2-nitrobenzoic acid | [CAS]
610-37-7 | [Synonyms]
3-carboxy-4-nitrophenol
5-HYDROXY-2-NITROBENZOIC ACID
RARECHEM AL BE 0679
5-hydroxy-2-nitro-benzoicaci
5-Hydroxy-2-nitrobenzoic acid, tech
2-Nitro-5-hydroxybenzoic acid | [Molecular Formula]
C7H5NO5 | [MDL Number]
MFCD00017566 | [Molecular Weight]
183.12 | [MOL File]
610-37-7.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection . | [Hazard Note ]
Irritant | [HS Code ]
29163990 |
| Hazard Information | Back Directory | [Uses]
5-Hydroxy-2-nitrobenzoic acid inhibits the activity of wild type-bovine low Mr protein tyrosine phosphatase. The inhibition constant has been evaluated. | [Synthesis]
General procedure for the synthesis of 2-nitro-5-hydroxybenzoic acid from 5-chloro-2-nitrobenzoic acid: 5-chloro-2-nitrobenzoic acid (32.00 g, 0.159 mol) was dissolved in 15% aqueous sodium hydroxide solution and reacted at reflux under nitrogen protection for 72 hours. After completion of the reaction, the pH of the reaction solution was adjusted to 1.0 with dilute hydrochloric acid and then extracted with ethyl acetate. The ethyl acetate extracts were combined and dried with anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure to give 28.05 g of 2-nitro-5-hydroxybenzoic acid in 96.5% yield. | [References]
[1] Chemistry - A European Journal, 2013, vol. 19, # 43, p. 14654 - 14664
[2] Patent: CN106478548, 2017, A. Location in patent: Paragraph 0019-0020; 0035-0036; 0051-0052; 0067-0068
[3] Patent: US2017/158680, 2017, A1. Location in patent: Paragraph 0330; 0331; 0332
[4] Patent: WO2003/97641, 2003, A2. Location in patent: Page/Page column 63
[5] Patent: US4348396, 1982, A |
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