RARECHEM AK ML 0025
Quinoline-5-carbaldehyde
CAS: 22934-41-4
Molecular Formula: C10H7NO
RARECHEM AK ML 0025 - Names and Identifiers
| Name | Quinoline-5-carbaldehyde |
| Synonyms | 5-Formylquinoline RARECHEM AK ML 0025 CHEMBRDG-BB 4300479 5-Quinolinecarbaldehyde Quinoline-5-carbaldehyde Quinoline-5-carboxaldehyde Quinoline-5-carbaldehyde(QUC) 5-Formylquinoline, 5-Formyl-1-azanaphthalene |
| CAS | 22934-41-4 |
| EINECS | 681-853-1 |
| InChI | InChI=1/C10H7NO/c12-7-8-3-1-5-10-9(8)4-2-6-11-10/h1-7H |
RARECHEM AK ML 0025 - Physico-chemical Properties
| Molecular Formula | C10H7NO |
| Molar Mass | 157.17 |
| Density | 1.223±0.06 g/cm3(Predicted) |
| Melting Point | 95-96°C |
| Boling Point | 314.3±15.0 °C(Predicted) |
| Flash Point | 151.9°C |
| Water Solubility | Slightly soluble in water. |
| Vapor Presure | 0.00047mmHg at 25°C |
| BRN | 113095 |
| pKa | 3.94±0.12(Predicted) |
| Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
| Sensitive | Air Sensitive |
| Refractive Index | 1.687 |
| MDL | MFCD00805835 |
RARECHEM AK ML 0025 - Risk and Safety
| Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin. R43 - May cause sensitization by skin contact |
| 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. S36/37 - Wear suitable protective clothing and gloves. |
| Hazard Class | IRRITANT |
RARECHEM AK ML 0025 - Introduction
Quinoline-5-carbaldehyde, also known as Quinoline-5-carbaldehyde, is an organic compound. Its chemical formula is C10H7CHO, and its structure has a quinoline ring and a formaldehyde group.
Nature:
Quinoline-5-carbaldehyde is a colorless liquid with a strong pungent odor. It is soluble in many organic solvents such as alcohols, ethers and ketones. This compound undergoes an oxidation reaction in sunlight.
Use:
Quinoline-5-carbaldehyde are widely used in the field of organic synthesis. It is an important intermediate in the synthesis of other organic compounds. In addition, it is also used as a raw material for dyes and paints, as well as a starting material for the manufacture of pharmaceuticals and pesticides.
Method:
Quinoline-5-carbaldehyde can be synthesized by a variety of methods, one of the commonly used methods is obtained from 5-quinolinol through oxidation reaction. Other synthetic methods include redox reaction, chlorination reaction and acylation reaction.
Safety Information:
Quinoline-5-carbaldehyde are irritating and flammable liquids. During use, care should be taken to avoid contact with skin, eyes and respiratory tract. Appropriate protective equipment such as gloves, goggles and respiratory protection should be worn. During storage and handling, appropriate safe operating procedures should be followed to avoid flames and high temperature sources.
Nature:
Quinoline-5-carbaldehyde is a colorless liquid with a strong pungent odor. It is soluble in many organic solvents such as alcohols, ethers and ketones. This compound undergoes an oxidation reaction in sunlight.
Use:
Quinoline-5-carbaldehyde are widely used in the field of organic synthesis. It is an important intermediate in the synthesis of other organic compounds. In addition, it is also used as a raw material for dyes and paints, as well as a starting material for the manufacture of pharmaceuticals and pesticides.
Method:
Quinoline-5-carbaldehyde can be synthesized by a variety of methods, one of the commonly used methods is obtained from 5-quinolinol through oxidation reaction. Other synthetic methods include redox reaction, chlorination reaction and acylation reaction.
Safety Information:
Quinoline-5-carbaldehyde are irritating and flammable liquids. During use, care should be taken to avoid contact with skin, eyes and respiratory tract. Appropriate protective equipment such as gloves, goggles and respiratory protection should be worn. During storage and handling, appropriate safe operating procedures should be followed to avoid flames and high temperature sources.
Last Update：2024-04-09 19:05:48
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CAS: 22934-41-4
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