135242-71-6
3-HYDROXY-4-IODOBENZALDEHYDE
CAS: 135242-71-6
Molecular Formula: C7H5IO2
135242-71-6 - Names and Identifiers
| Name | 3-HYDROXY-4-IODOBENZALDEHYDE |
| Synonyms | RARECHEM AX KI 1030 5-Formyl-2-iodophenol 3-HYDROXY-4-IODOBENZALDEHYDE Benzaldehyde, 3-hydroxy-4-iodo- [1-(2-methoxy-1-naphthalenyl)-2-naphthalenyl]-diphenylphosphine |
| CAS | 135242-71-6 |
| InChI | InChI=1/C7H5IO2/c8-6-2-1-5(4-9)3-7(6)10/h1-4,10H |
135242-71-6 - Physico-chemical Properties
| Molecular Formula | C7H5IO2 |
| Molar Mass | 248.02 |
| Density | 2.039±0.06 g/cm3(Predicted) |
| Melting Point | 126-128 |
| Boling Point | 252.2±25.0 °C(Predicted) |
| Flash Point | 106.357°C |
| Vapor Presure | 0.012mmHg at 25°C |
| pKa | 7.79±0.10(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1.715 |
135242-71-6 - Risk and Safety
| Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin. R43 - May cause sensitization by skin contact R41 - Risk of serious damage to eyes R22 - Harmful if swallowed |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S66 - S22 - Do not breathe dust. S36/37 - Wear suitable protective clothing and gloves. |
| Hazard Note | Irritant |
135242-71-6 - Reference Information
| Use | 3-hydroxy-4-iodobenzaldehyde is white to off-white solid at room temperature and pressure, 3-hydroxy-4-iodobenzaldehyde is a benzaldehyde derivative, which is oxidized by air for a long time to generate corresponding benzoic acid compounds. 3-hydroxy-4-iodobenzaldehyde is commonly used as an intermediate in medical chemistry and organic synthesis, it can be used for synthetic herbicides and plant growth regulators. |
| Synthesis method | Add 3-hydroxy -2,4, 6-triiodobenzaldehyde, dry pyridine and catalytic amount to the dry reaction bottle The obtained mixture is stirred for 4 hours in a reflux state. After the reaction is over, the mixture is concentrated in a vacuum state, the residue was then purified by silica gel column chromatography and eluted with (petroleum ether: ethyl acetate = 4:1(v/v)) to obtain the target product 3-hydroxy-4-iodobenzaldehyde. Figure 3-Hydroxy-4-iodobenzaldehyde synthesis route |
Last Update：2024-04-09 21:01:54
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