3993-57-5
4-methyl-7-(prop-2-en-1-yloxy)-2H-chromen-2-one
CAS: 3993-57-5
Molecular Formula: C13H12O3
3993-57-5 - Names and Identifiers
| Name | 4-methyl-7-(prop-2-en-1-yloxy)-2H-chromen-2-one |
| Synonyms | 7-ALLYLOXY-4-METHYLCOUMARIN 4-methyl-7-prop-2-enoxychromen-2-one 4-methyl-7-prop-2-enoxy-chromen-2-one 4-methyl-7-(prop-2-en-1-yloxy)-2H-chromen-2-one 2H-1-Benzopyran-2-one, 4-methyl-7-(2-propen-1-yloxy)- |
| CAS | 3993-57-5 |
| InChI | InChI=1/C13H12O3/c1-3-6-15-10-4-5-11-9(2)7-13(14)16-12(11)8-10/h3-5,7-8H,1,6H2,2H3 |
3993-57-5 - Physico-chemical Properties
| Molecular Formula | C13H12O3 |
| Molar Mass | 216.23 |
| Density | 1.155g/cm3 |
| Boling Point | 373.1°C at 760 mmHg |
| Flash Point | 156.4°C |
| Vapor Presure | 9.19E-06mmHg at 25°C |
| Refractive Index | 1.555 |
3993-57-5 - Introduction
4-methyl-7-(prop-2-en-1-yloxy)-2H-chromen-2-one is a compound with the formula C15H14O3. This is a yellow crystalline powder, soluble in some organic solvents.
It is mainly used for the synthesis of fluorescent probes and related research. Because of its blue fluorescence characteristics, it can be used in cells and organisms for fluorescence imaging, cell tracing, biosensing and other aspects of the study.
The synthesis method of 4-methyl-7-(prop-2-en-1-yloxy)-2H-chromen-2-one is generally carried out by a chemical synthesis method. A common preparation method is to react 4-methylcoumarin with allyl alcohol, and the reaction is promoted by an alkyd catalyst to produce 4-methyl-7-(prop-2-en-1-yloxy)-2H-chromen-2-one.
Regarding safety information, 4-methyl-7-(prop-2-en-1-yloxy)-2H-chromen-2-one has low toxicity, but it still needs to be used with caution. Avoid contact with skin and eyes during operation, and avoid inhaling its dust. Operate in a well-ventilated area and wear appropriate protective equipment such as lab gloves, goggles, etc.
In general, 4-methyl-7-(prop-2-en-1-yloxy)-2H-chromen-2-one is a commonly used fluorescent probe compound, which has certain experimental application value. However, when using, it is still necessary to operate in accordance with the safety operation procedures of chemicals to ensure the safety of the experiment.
It is mainly used for the synthesis of fluorescent probes and related research. Because of its blue fluorescence characteristics, it can be used in cells and organisms for fluorescence imaging, cell tracing, biosensing and other aspects of the study.
The synthesis method of 4-methyl-7-(prop-2-en-1-yloxy)-2H-chromen-2-one is generally carried out by a chemical synthesis method. A common preparation method is to react 4-methylcoumarin with allyl alcohol, and the reaction is promoted by an alkyd catalyst to produce 4-methyl-7-(prop-2-en-1-yloxy)-2H-chromen-2-one.
Regarding safety information, 4-methyl-7-(prop-2-en-1-yloxy)-2H-chromen-2-one has low toxicity, but it still needs to be used with caution. Avoid contact with skin and eyes during operation, and avoid inhaling its dust. Operate in a well-ventilated area and wear appropriate protective equipment such as lab gloves, goggles, etc.
In general, 4-methyl-7-(prop-2-en-1-yloxy)-2H-chromen-2-one is a commonly used fluorescent probe compound, which has certain experimental application value. However, when using, it is still necessary to operate in accordance with the safety operation procedures of chemicals to ensure the safety of the experiment.
Last Update：2024-04-10 22:29:15
