QUINOCETONE
Quinocetone
CAS: 81810-66-4
Molecular Formula: C18H14N2O3
QUINOCETONE - Names and Identifiers
| Name | Quinocetone |
| Synonyms | kuixitong QUINOCETONE Quinocetone 2-Cinnamoyl-3-methylquinoxaline 1,4-dioxide 1-(3-Methyl-1,4-dioxido-2-quinoxalinyl)-3-phenyl-2-propen-1-one 1-(3-Methyl-2-quinoxalinyl)-3-phenyl-2-propen-1-one N,N'-dioxide 2-Propen-1-one, 1-(3-methyl-1,4-dioxido-2-quinoxalinyl)-3-phenyl- 1-(3-Methyl-2-quinoxalinyl)-3-phenyl-2-propen-1-one N,N'-dioxide (E)-1-(3-methyl-4-oxido-1-oxo-2-quinoxalin-1-iumyl)-3-phenyl-2-propen-1-one |
| CAS | 81810-66-4 |
| EINECS | 1312995-182-4 |
QUINOCETONE - Physico-chemical Properties
| Molecular Formula | C18H14N2O3 |
| Molar Mass | 306.32 |
| Density | 1.22 |
| Melting Point | 183-188 °C |
| Boling Point | 576.9±60.0 °C(Predicted) |
| Solubility | Insoluble in water, slightly soluble in some organic solvents |
| Appearance | Pale yellow or yellow green powder |
| Color | Yellow |
| pKa | 1.62±0.30(Predicted) |
| Storage Condition | 2-8°C |
| MDL | MFCD09753267 |
QUINOCETONE - Reference
| Reference Show more | 1. Xiaoyun Bai, Bo Zhang, Miao Liu, Xuelian Hu, Guozhen Fang, Shuo Wang, Molecularly imprinted electrochemical sensor based on polypyrrole/dopamine@graphene incorporated with surface molecularly imprinted polymers thin film for recognition of olaquindox, Bioe 2. [IF=5.373] Xiaoyun Bai et al."Molecularly imprinted electrochemical sensor based on polypyrrole/dopamine@graphene incorporated with surface molecularly imprinted polymers thin film for recognition of olaquindox."Bioelectrochemistry. 2020 Apr;132:107398 |
QUINOCETONE - Introduction
Quinocetones (quinones) are a class of organic compounds containing Quinone groups. It has the following main properties:
1. Color: Quinocetone presents a dark yellow to brown solid or orange to reddish-brown crystal.
2. Odor: it usually has a pungent smell.
3. Solubility: Quinocetone has good solubility in non-polar solvents, such as chloroform, benzene and ether. However, the solubility in water is poor.
Quinocetone has a wide range of uses, including but not limited to the following:
1. Chemical Synthesis: Quinocetone can be used as an oxidant to participate in organic synthesis reactions, such as oxidation of alcohols, aldehydes, amines and sulfides. It can also be used in the synthesis of dyes, drugs and other organic compounds.
2. Photosensitive material: Quinocetone can be used as photosensitive material for photosensitive body, photosensitizer and other applications. It can carry out important electron transfer reactions under the excitation of visible light and ultraviolet light.
3. Fuel cells: Quinocetone and its derivatives can be used in dye-sensitized solar cells and other optoelectronic devices.
There are many ways to make Quinocetone, the common ones include:
1. Oxidation method: Quinocetone can be prepared by reacting the corresponding diphenol or aromatic amine with oxygen or an oxidant.
2. Reduction method: Quinocetone can be obtained by reducing the corresponding quinone.
Quinocetone has certain security risks, you need to pay attention to the following points:
1. Toxicity: Quinocetone has a certain toxicity, contact or inhalation of Quinocetone may cause irritation, eye and skin inflammation and other reactions.
2. Stability: Quinocetone is easy to decompose under light, and avoiding exposure to strong light can extend its stability.
3. Protective measures: When operating Quinocetone, appropriate protective measures should be taken, including wearing protective glasses, gloves and protective clothing. At the same time, ensure that the operating environment is well ventilated.
1. Color: Quinocetone presents a dark yellow to brown solid or orange to reddish-brown crystal.
2. Odor: it usually has a pungent smell.
3. Solubility: Quinocetone has good solubility in non-polar solvents, such as chloroform, benzene and ether. However, the solubility in water is poor.
Quinocetone has a wide range of uses, including but not limited to the following:
1. Chemical Synthesis: Quinocetone can be used as an oxidant to participate in organic synthesis reactions, such as oxidation of alcohols, aldehydes, amines and sulfides. It can also be used in the synthesis of dyes, drugs and other organic compounds.
2. Photosensitive material: Quinocetone can be used as photosensitive material for photosensitive body, photosensitizer and other applications. It can carry out important electron transfer reactions under the excitation of visible light and ultraviolet light.
3. Fuel cells: Quinocetone and its derivatives can be used in dye-sensitized solar cells and other optoelectronic devices.
There are many ways to make Quinocetone, the common ones include:
1. Oxidation method: Quinocetone can be prepared by reacting the corresponding diphenol or aromatic amine with oxygen or an oxidant.
2. Reduction method: Quinocetone can be obtained by reducing the corresponding quinone.
Quinocetone has certain security risks, you need to pay attention to the following points:
1. Toxicity: Quinocetone has a certain toxicity, contact or inhalation of Quinocetone may cause irritation, eye and skin inflammation and other reactions.
2. Stability: Quinocetone is easy to decompose under light, and avoiding exposure to strong light can extend its stability.
3. Protective measures: When operating Quinocetone, appropriate protective measures should be taken, including wearing protective glasses, gloves and protective clothing. At the same time, ensure that the operating environment is well ventilated.
Last Update：2024-04-10 22:43:14
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