5-Cyano-1-indanone
5-Cyano-1-indanone
CAS: 25724-79-2
Molecular Formula: C10H7NO
5-Cyano-1-indanone - Names and Identifiers
5-Cyano-1-indanone - Physico-chemical Properties
| Molecular Formula | C10H7NO |
| Molar Mass | 157.17 |
| Density | 1.23±0.1 g/cm3(Predicted) |
| Melting Point | 128-130 °C |
| Boling Point | 325.6±31.0 °C(Predicted) |
| Flash Point | 150.7°C |
| Vapor Presure | 0.000228mmHg at 25°C |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1.596 |
5-Cyano-1-indanone - Introduction
5-Cyano-1-indanone(5-Cyano-1-indanone) is an organic compound with the chemical formula C11H7NO. The following is an introduction to its nature, use, formulation and safety information:
Nature:
-Appearance: 5-Cyano-1-indanone is a white to light yellow solid.
-Melting point: about 82-85 degrees Celsius.
-Solubility: Can be dissolved in most organic solvents, such as ethanol, methanol, chloroform, etc.
-Stability: relatively stable, not easy to decompose at room temperature.
-chemical reaction: the characteristics of carbonyl compounds, prone to addition, condensation, acid-base reaction.
Use:
-Chemical synthesis: 5-Cyano-1-indanone is a commonly used organic synthesis intermediate, which can be used to synthesize other organic compounds, such as drugs, dyes and pesticides.
-Research: It is also commonly used in laboratory research of organic synthesis reactions.
Method:
The preparation method of 5-Cyano-1-indanone can use vanillin as a raw material to carry out the following reaction steps:
1. Under alkaline conditions, vanillin reacts with sodium cyanide to generate 5-cyano-1-indanone.
2. 5-Cyano-1-indanone is then oxidized under acidic conditions to give 5-Cyano-1-indanone.
Safety Information:
5-Cyano-1-indanone should be used and stored in accordance with regular laboratory safety procedures. Note the following safety information:
-the skin, eyes and mucous membrane irritation, contact should be avoided.
-May be harmful to the respiratory tract and digestive tract, should avoid inhalation and ingestion.
-It needs to be used in a well-ventilated area and equipped with appropriate personal protective equipment, such as gloves, goggles, etc.
-It should be stored in a dry, cool place to avoid contact with oxidants and other substances.
-Observe local regulations and environmental protection requirements during handling and disposal.
Nature:
-Appearance: 5-Cyano-1-indanone is a white to light yellow solid.
-Melting point: about 82-85 degrees Celsius.
-Solubility: Can be dissolved in most organic solvents, such as ethanol, methanol, chloroform, etc.
-Stability: relatively stable, not easy to decompose at room temperature.
-chemical reaction: the characteristics of carbonyl compounds, prone to addition, condensation, acid-base reaction.
Use:
-Chemical synthesis: 5-Cyano-1-indanone is a commonly used organic synthesis intermediate, which can be used to synthesize other organic compounds, such as drugs, dyes and pesticides.
-Research: It is also commonly used in laboratory research of organic synthesis reactions.
Method:
The preparation method of 5-Cyano-1-indanone can use vanillin as a raw material to carry out the following reaction steps:
1. Under alkaline conditions, vanillin reacts with sodium cyanide to generate 5-cyano-1-indanone.
2. 5-Cyano-1-indanone is then oxidized under acidic conditions to give 5-Cyano-1-indanone.
Safety Information:
5-Cyano-1-indanone should be used and stored in accordance with regular laboratory safety procedures. Note the following safety information:
-the skin, eyes and mucous membrane irritation, contact should be avoided.
-May be harmful to the respiratory tract and digestive tract, should avoid inhalation and ingestion.
-It needs to be used in a well-ventilated area and equipped with appropriate personal protective equipment, such as gloves, goggles, etc.
-It should be stored in a dry, cool place to avoid contact with oxidants and other substances.
-Observe local regulations and environmental protection requirements during handling and disposal.
Last Update：2024-04-09 19:05:48
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View History
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telluriumoxide(teo2)
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