301836-57-7
2,3-dihydro-1-benzofuran-6-carboxylic acid
CAS: 301836-57-7
Molecular Formula: C9H8O3
301836-57-7 - Names and Identifiers
| Name | 2,3-dihydro-1-benzofuran-6-carboxylic acid |
| Synonyms | 2,3-dihydrobenzofuran-6-carboxylic acid 6-Benzofurancarboxylic acid, 2,3-dihydro- 6-benzofurancarboxylic acid, 2,3-dihydro- 2,3-dihydro-1-benzofuran-6-carboxylic acid |
| CAS | 301836-57-7 |
| InChI | InChI=1/C9H8O3/c10-9(11)7-2-1-6-3-4-12-8(6)5-7/h1-2,5H,3-4H2,(H,10,11) |
301836-57-7 - Physico-chemical Properties
| Molecular Formula | C9H8O3 |
| Molar Mass | 164.16 |
| Density | 1.344±0.06 g/cm3(Predicted) |
| Boling Point | 322.8±31.0 °C(Predicted) |
| Flash Point | 136°C |
| Vapor Presure | 0.000112mmHg at 25°C |
| pKa | 4.25±0.20(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1.61 |
301836-57-7 - Introduction
2. acid is an organic compound with the chemical formula C9H8O3.
Nature:
2, acid is a colorless crystalline solid with a special aromatic flavor. It is insoluble in water at room temperature, but soluble in organic solvents such as ethanol and dichloromethane.
Use:
2, acid plays an important role in drug synthesis. It can be used for the synthesis of other drug intermediates, and can also be used as the structural skeleton of drugs.
Method:
2. The synthesis of acid can be obtained by the reaction of benzyl alcohol and 2,3-dihydrofuran. First, benzyl alcohol and 2,3-dihydrofuran undergo an alcohol ether exchange reaction under alkaline conditions to produce 2-benzyl -2, 3-dihydrofuran. Then, 2-benzyl-2,3-dihydrofuran undergoes an acid hydrolysis reaction to give 2, acid.
Safety Information:
2, acid has no obvious danger under regular use. However, as an organic compound, it may have irritating effects on the skin, eyes and respiratory system, so care should be taken to avoid contact when using it. Wear appropriate personal protective equipment such as lab gloves and goggles when used in a laboratory environment. In addition, the compound should be stored and handled properly to avoid reaction with other chemicals, fire and high temperatures.
Nature:
2, acid is a colorless crystalline solid with a special aromatic flavor. It is insoluble in water at room temperature, but soluble in organic solvents such as ethanol and dichloromethane.
Use:
2, acid plays an important role in drug synthesis. It can be used for the synthesis of other drug intermediates, and can also be used as the structural skeleton of drugs.
Method:
2. The synthesis of acid can be obtained by the reaction of benzyl alcohol and 2,3-dihydrofuran. First, benzyl alcohol and 2,3-dihydrofuran undergo an alcohol ether exchange reaction under alkaline conditions to produce 2-benzyl -2, 3-dihydrofuran. Then, 2-benzyl-2,3-dihydrofuran undergoes an acid hydrolysis reaction to give 2, acid.
Safety Information:
2, acid has no obvious danger under regular use. However, as an organic compound, it may have irritating effects on the skin, eyes and respiratory system, so care should be taken to avoid contact when using it. Wear appropriate personal protective equipment such as lab gloves and goggles when used in a laboratory environment. In addition, the compound should be stored and handled properly to avoid reaction with other chemicals, fire and high temperatures.
Last Update：2024-04-09 21:01:54
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