4-QUINOLINEACETICACID
Indole-3-carboxaldehyde
CAS: 487-89-8;4877-89-8
Molecular Formula: C9H7NO
4-QUINOLINEACETICACID - Names and Identifiers
4-QUINOLINEACETICACID - Physico-chemical Properties
| Molecular Formula | C9H7NO |
| Molar Mass | 145.16 |
| Density | 1.1555 (rough estimate) |
| Melting Point | 193-198°C(lit.) |
| Boling Point | 264.27°C (rough estimate) |
| Flash Point | 240 °C |
| Water Solubility | Insoluble in water. |
| Solubility | Slightly soluble in water |
| Vapor Presure | 9.42E-05mmHg at 25°C |
| Appearance | White-like crystal |
| Color | Off-white to beige-brown |
| BRN | 114117 |
| pKa | 15.50±0.30(Predicted) |
| Storage Condition | Store below +30°C. |
| Stability | Hygroscopic |
| Sensitive | Air Sensitive |
| Refractive Index | 1.4500 (estimate) |
| MDL | MFCD00005622 |
| Physical and Chemical Properties | The trait has the general properties of aromatic aldehydes. melting point 195 ℃ |
| Use | For the preparation of indole derivatives |
4-QUINOLINEACETICACID - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| RTECS | NL5993600 |
| FLUKA BRAND F CODES | 9-23 |
| TSCA | Yes |
| HS Code | 29339990 |
| Hazard Note | Irritant/Keep Cold |
| Hazard Class | IRRITANT |
4-QUINOLINEACETICACID - Introduction
Insoluble in water
Last Update：2022-10-16 17:25:25
4-QUINOLINEACETICACID - Reference Information
| NIST chemical information | Information provided by: webbook.nist.gov (external link) |
| EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
| overview | the chemical structural formula of 3-indole formaldehyde is as follows, its molecular formula is C9H7NO, and its relative molecular weight is 145.161. It has been reported that 3-indole formaldehyde has certain antibacterial, anti-inflammatory and anti-tumor biological activities. In addition, 3-indole formaldehyde is also an important pharmaceutical and organic intermediate, which can be used to synthesize many compounds with physiological and pharmacological activities, such as indole acetic acid, indomethacin, etc. At present, one of the main sources of 3-indole formaldehyde is chemical synthesis, but the chemical synthesis process is more complicated, involving many toxic and harmful reagents, and the yield is limited; another way is to extract from natural plants, and there is also the problem of cumbersome extraction process and low yield. At present, the method of extracting 3-indole formaldehyde from ascidians has not been reported. |
| use | it has been reported that 3-indole formaldehyde has certain antibacterial, anti-inflammatory and anti-tumor biological activities. in addition, 3-indole formaldehyde is also an important pharmaceutical and organic intermediate, and can be used to synthesize many compounds with physiological and pharmacological activities, such as indole acetic acid, indomethacin, etc. for the preparation of indole derivatives organic synthesis pharmaceutical intermediates; for the synthesis of high-order indole starting materials, including isoindolo[2,1-a]indoles,aplysinopsins and 4-substituted tetrahydrobenz[cd]indoles |
| spontaneous combustion temperature | >550°C |
Last Update：2024-04-09 02:00:08
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