1H-Isoindole-1,3(2H)-dione,2-(4-hydroxycyclohexyl)
4 (phthalimide) Cyclohexanol
CAS: 104618-31-7
Molecular Formula: C14H15NO3
1H-Isoindole-1,3(2H)-dione,2-(4-hydroxycyclohexyl) - Names and Identifiers
| Name | 4 (phthalimide) Cyclohexanol |
| Synonyms | 4-(Phthalimide)cyclohexanol 4 (phthalimide) Cyclohexanol 2-(4-Hydroxycyclohexyl)isoindol-1,3-dione 2-(4-Hydroxycyclohexyl)isoindoline-1,3-dione 1H-Isoindole-1,3(2H)-dione,2-(4-hydroxycyclohexyl) 2-(4-Hydroxycyclohexyl)-1H-isoindole-1,3(2H)-dione |
| CAS | 104618-31-7 |
| EINECS | 1533716-785-6 |
| InChI | InChI=1S/C14H15NO3/c16-10-7-5-9(6-8-10)15-13(17)11-3-1-2-4-12(11)14(15)18/h1-4,9-10,16H,5-8H2 |
1H-Isoindole-1,3(2H)-dione,2-(4-hydroxycyclohexyl) - Physico-chemical Properties
| Molecular Formula | C14H15NO3 |
| Molar Mass | 245.27 |
| Density | 1.365 |
| Boling Point | 410.1±38.0 °C(Predicted) |
| pKa | 14.99±0.40(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
1H-Isoindole-1,3(2H)-dione,2-(4-hydroxycyclohexyl) - Introduction
2-(4-Hydroxycyclohexyl) isoindole -1, 3-dione, also known as calcium, is an organic compound. The following is a description of its nature, use, formulation and safety information:
Nature:
-Appearance: 2-(4-Hydroxycyclohexyl) isoindol-1, 3-dione is a white to light yellow crystalline solid.
-Solubility: It is easily soluble in some organic solvents such as ethanol, dimethyl sulfoxide and dichloromethane, but it is poorly soluble in water.
Use:
-Chemical reagent: 2-(4-hydroxycyclohexyl) isoindol-1, 3-dione is commonly used as a reagent in organic synthesis, especially in the field of pharmaceutical synthesis.
-Pharmaceutical field: It is also used in the research of bioactive molecules and drug discovery, and can be used as a precursor or intermediate of potential drug molecules.
Preparation Method:
2-(4-Hydroxycyclohexyl) isoindol-1, 3-dione can be synthesized by the following steps:
1. the reaction of 2-amino indole with 4-hydroxy cyclohexanone to generate the corresponding ketone alcohol intermediate.
2. After deprotection reaction, the protecting group is removed to obtain 2-(4-hydroxycyclohexyl) isoindole -1, 3-dione.
Safety Information:
- 2-(4-Hydroxycyclohexyl) isoindol-1, 3-dione has no apparent toxicity or danger when used under routine laboratory conditions.
-However, as a chemical, it is important to follow routine safety procedures when handling, including wearing appropriate personal protective equipment, avoiding contact with skin and eyes, and avoiding inhalation or ingestion.
-When using or storing, it should be stored in a sealed container, away from fire and oxidizing agents.
Nature:
-Appearance: 2-(4-Hydroxycyclohexyl) isoindol-1, 3-dione is a white to light yellow crystalline solid.
-Solubility: It is easily soluble in some organic solvents such as ethanol, dimethyl sulfoxide and dichloromethane, but it is poorly soluble in water.
Use:
-Chemical reagent: 2-(4-hydroxycyclohexyl) isoindol-1, 3-dione is commonly used as a reagent in organic synthesis, especially in the field of pharmaceutical synthesis.
-Pharmaceutical field: It is also used in the research of bioactive molecules and drug discovery, and can be used as a precursor or intermediate of potential drug molecules.
Preparation Method:
2-(4-Hydroxycyclohexyl) isoindol-1, 3-dione can be synthesized by the following steps:
1. the reaction of 2-amino indole with 4-hydroxy cyclohexanone to generate the corresponding ketone alcohol intermediate.
2. After deprotection reaction, the protecting group is removed to obtain 2-(4-hydroxycyclohexyl) isoindole -1, 3-dione.
Safety Information:
- 2-(4-Hydroxycyclohexyl) isoindol-1, 3-dione has no apparent toxicity or danger when used under routine laboratory conditions.
-However, as a chemical, it is important to follow routine safety procedures when handling, including wearing appropriate personal protective equipment, avoiding contact with skin and eyes, and avoiding inhalation or ingestion.
-When using or storing, it should be stored in a sealed container, away from fire and oxidizing agents.
Last Update：2024-04-09 20:45:29
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