Identification | More | [Name]
5-Hydroxy-2-nitrobenzaldehyde | [CAS]
42454-06-8 | [Synonyms]
2-NITRO-5-HYDROXYBENZALDEHYDE 3-HYDROXY-6-NITROBENZALDEHYDE 5-HYDROXY-2-NITROBENZALDEHYDE 6-NITRO-3-HYDROXYBENZALDEHYDE 6-NITRO-3-HYDROXY BENZALDHYDE LABOTEST-BB LT00233113 3-Formyl-4-nitrophenol 5-hydroxy-2-nitro-benzaldehyd Benzaldehyde, 5-hydroxy-2-nitro- 2-NITRO-5-HYDROXYBENZALDE 5-Hydroxy-2-nitrobenzaldehy 5-HYDROXY-2-NITROBENZALDEHYDE 98+% | [EINECS(EC#)]
255-832-9 | [Molecular Formula]
C7H5NO4 | [MDL Number]
MFCD00007332 | [Molecular Weight]
167.12 | [MOL File]
42454-06-8.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 . S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [RTECS ]
CU6700000
| [HS Code ]
29130000 |
Hazard Information | Back Directory | [Chemical Properties]
Yellow powder | [Uses]
5-Hydroxy-2-nitrobenzaldehyde is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff. | [Synthesis Reference(s)]
The Journal of Organic Chemistry, 44, p. 409, 1979 DOI: 10.1021/jo01317a021 | [Synthesis]
The general procedure for the synthesis of 5-hydroxy-2-nitrobenzaldehyde (formula VI) using m-hydroxybenzaldehyde (formula V, R5=H) as starting material was as follows: 3 g of m-hydroxybenzaldehyde was slowly added to 30 ml of nitric acid (density = 1.17, 28% solution), and the temperature of the solution was maintained at a temperature between 35°C and 45°C during the reaction. After the addition was completed, hydrolysis was carried out and the reaction mixture was subsequently left to stand at room temperature. The reaction produced a yellow precipitate which was filtered and the precipitate was refluxed in 20 ml of benzene for 15 to 20 minutes. The insoluble material was separated and purified by recrystallization in water. 5-Hydroxy-2-nitrobenzaldehyde (formula VI) was finally obtained in 25% yield with a melting point of 167°C (molecular formula: C7H5NO4, molecular weight = 167). | [References]
[1] Helvetica Chimica Acta, 1992, vol. 75, # 4, p. 1185 - 1197 [2] Patent: US5139707, 1992, A [3] Bioorganic and Medicinal Chemistry, 2016, vol. 24, # 3, p. 444 - 452 [4] Journal of the Chemical Society, 1925, vol. 127, p. 2171 [5] Journal of the Chemical Society, 1925, vol. 127, p. 876,877 |
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