4,5-di(morpholin-4-yl)cyclohexa-3,5-diene-1,2-dione
4,5-Dimorpholin-4-ylbenzo-1,2-quinone
CAS: 4608-10-0
Molecular Formula: C14H18N2O4
4,5-di(morpholin-4-yl)cyclohexa-3,5-diene-1,2-dione - Names and Identifiers
4,5-di(morpholin-4-yl)cyclohexa-3,5-diene-1,2-dione - Physico-chemical Properties
| Molecular Formula | C14H18N2O4 |
| Molar Mass | 278.3 |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD01366762 |
4,5-di(morpholin-4-yl)cyclohexa-3,5-diene-1,2-dione - Risk and Safety
| Hazard Class | IRRITANT |
4,5-di(morpholin-4-yl)cyclohexa-3,5-diene-1,2-dione - Introduction
4. 2-quinone (4,5-dimorpholinylbenzoquinoline -1,2-one) is a compound with the following properties:
-Appearance: 4, 2-quinone is white to light yellow crystal or powder form.
-Solubility: It is soluble in some organic solvents, such as ethanol, dimethyl sulfoxide and ethers.
-Melting point: Its melting point is higher, generally around 110-115°C.
-Structure: Its molecular structure contains two morpholine groups and a benzoquinoline structure.
In chemistry, 4, and 2-quinone are mainly used as reagents and intermediates in organic synthesis. It can be used to synthesize other organic compounds, such as drugs, dyes and ligands. Its two morpholine groups can provide good coordination properties, especially in the transition metal catalytic reaction has a wide range of applications.
There are two main methods for preparing 4, 2-quinone. One is through the double acylation reaction of benzene ring, 2,5-dibromo acetic acid and 4,5-dimorpholinyl phenol reaction, and then through the acid hydrolysis, dehydration and oxidation steps to obtain the target product. The other is through the benzene ring nitrogen generation alkylation reaction, 4,5-dimethylaminophenol and diiodomethane reaction, and then through the acid hydrolysis, dehydration and oxidation steps.
Regarding the safety information of 4, 2-quinone, there is no clear toxicity and danger data at present. However, as a chemical substance, it needs to comply with general laboratory safety procedures, such as wearing appropriate protective equipment (such as gloves and glasses), avoiding inhalation, contact with skin and eyes, etc.
When conducting experiments or applications, it is best to follow reliable literature and reasonable experimental operation guidelines. For further information on the safety of this compound, it is recommended to consult the relevant data and resources.
-Appearance: 4, 2-quinone is white to light yellow crystal or powder form.
-Solubility: It is soluble in some organic solvents, such as ethanol, dimethyl sulfoxide and ethers.
-Melting point: Its melting point is higher, generally around 110-115°C.
-Structure: Its molecular structure contains two morpholine groups and a benzoquinoline structure.
In chemistry, 4, and 2-quinone are mainly used as reagents and intermediates in organic synthesis. It can be used to synthesize other organic compounds, such as drugs, dyes and ligands. Its two morpholine groups can provide good coordination properties, especially in the transition metal catalytic reaction has a wide range of applications.
There are two main methods for preparing 4, 2-quinone. One is through the double acylation reaction of benzene ring, 2,5-dibromo acetic acid and 4,5-dimorpholinyl phenol reaction, and then through the acid hydrolysis, dehydration and oxidation steps to obtain the target product. The other is through the benzene ring nitrogen generation alkylation reaction, 4,5-dimethylaminophenol and diiodomethane reaction, and then through the acid hydrolysis, dehydration and oxidation steps.
Regarding the safety information of 4, 2-quinone, there is no clear toxicity and danger data at present. However, as a chemical substance, it needs to comply with general laboratory safety procedures, such as wearing appropriate protective equipment (such as gloves and glasses), avoiding inhalation, contact with skin and eyes, etc.
When conducting experiments or applications, it is best to follow reliable literature and reasonable experimental operation guidelines. For further information on the safety of this compound, it is recommended to consult the relevant data and resources.
Last Update：2024-04-09 21:54:55
