cis-2-[(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)methyl-N,N-diethyl-1-phenylcyclopropanecarboxamide
cis-2-[(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)methyl-N,N-diethyl-1-phenylcyclopropanecarboxamide
CAS: 105310-75-6
Molecular Formula: C23H24N2O3
cis-2-[(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)methyl-N,N-diethyl-1-phenylcyclopropanecarboxamide - Names and Identifiers
cis-2-[(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)methyl-N,N-diethyl-1-phenylcyclopropanecarboxamide - Physico-chemical Properties
| Molecular Formula | C23H24N2O3 |
| Molar Mass | 376.45 |
| Density | 1.254 |
| Melting Point | 130-132°C |
| Boling Point | 546.1±29.0 °C(Predicted) |
| Flash Point | 236.1°C |
| Solubility | DMSO (Slightly), Methanol (Slightly) |
| Vapor Presure | 1.52E-11mmHg at 25°C |
| Appearance | Solid |
| Color | Off-White to Pale Beige |
| pKa | -0.68±0.40(Predicted) |
| Storage Condition | 2-8°C |
| Refractive Index | 1.638 |
cis-2-[(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)methyl-N,N-diethyl-1-phenylcyclopropanecarboxamide - Risk and Safety
| HS Code | 2925190100 |
cis-2-[(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)methyl-N,N-diethyl-1-phenylcyclopropanecarboxamide - Introduction
cis-2-[(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl) methyl-N, N-diethyl-1-phenylcyclopropanecarboxamide, also known as maleimide, is an organic compound. The following is a brief description of its nature, use, formulation and safety information:
Nature:
-maleimide is a white solid, stable at room temperature.
-It is an organic solvent, soluble in many organic solvents, such as alcohols, ethers and ketones.
-It has low volatility and low toxicity.
Use:
-maleimide is commonly used as an intermediate and reagent in organic synthesis.
-It can be used to synthesize organic compounds such as drugs, pesticides and functional materials.
-It can also be used as an additive for rubber, plastics, dyes and coatings.
Preparation Method:
-maleimide is usually obtained by reacting benzaldehyde with 1-pentene in the presence of sodium cyanide.
-Specific steps include cyanation, acidification, amidation and recrystallization.
Safety Information:
-The toxicity of maleimide is low, but it is still necessary to pay attention to reasonable use.
-During operation, avoid skin contact and inhalation of dust or vapor.
-eye and skin irritation, such as accidental contact, should immediately rinse with plenty of water and seek medical help.
-During storage and handling, keep away from fire and oxidizing agents, and ensure good ventilation.
Please note that the above is only a brief introduction. If you need to know more about its nature, use and safety information in specific applications, it is recommended to consult the relevant chemical literature or consult a professional.
Nature:
-maleimide is a white solid, stable at room temperature.
-It is an organic solvent, soluble in many organic solvents, such as alcohols, ethers and ketones.
-It has low volatility and low toxicity.
Use:
-maleimide is commonly used as an intermediate and reagent in organic synthesis.
-It can be used to synthesize organic compounds such as drugs, pesticides and functional materials.
-It can also be used as an additive for rubber, plastics, dyes and coatings.
Preparation Method:
-maleimide is usually obtained by reacting benzaldehyde with 1-pentene in the presence of sodium cyanide.
-Specific steps include cyanation, acidification, amidation and recrystallization.
Safety Information:
-The toxicity of maleimide is low, but it is still necessary to pay attention to reasonable use.
-During operation, avoid skin contact and inhalation of dust or vapor.
-eye and skin irritation, such as accidental contact, should immediately rinse with plenty of water and seek medical help.
-During storage and handling, keep away from fire and oxidizing agents, and ensure good ventilation.
Please note that the above is only a brief introduction. If you need to know more about its nature, use and safety information in specific applications, it is recommended to consult the relevant chemical literature or consult a professional.
Last Update：2024-04-09 15:17:50
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CAS: 105310-75-6
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CAS: 105310-75-6
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