19499-83-3
1H-Indol-4-ol, 5-methyl-
CAS: 19499-83-3
Molecular Formula: C9H9NO
19499-83-3 - Names and Identifiers
| Name | 1H-Indol-4-ol, 5-methyl- |
| Synonyms | 5-Methyl-1H-indol-4-ol 1H-Indol-4-ol, 5-Methyl- 1H-Indol-4-ol, 5-methyl- 4-Hydroxy-5-Methyl-indole 5-Methyl-4-hydroxy-1H-indole |
| CAS | 19499-83-3 |
19499-83-3 - Physico-chemical Properties
| Molecular Formula | C9H9NO |
| Molar Mass | 147.17 |
| Storage Condition | Room Temprature |
19499-83-3 - Introduction
1H-Indol-4-ol, 5-methyl-(5-Methyl-1H-indol-4-ol) is an organic compound with the chemical formula C9H9NO. It is a white or yellowish solid with a fragrant odor.
The main use of this compound is as an intermediate in organic synthesis. It can be used to synthesize various similar compounds, such as fluorescent dyes, drugs, natural products, etc.
The preparation method of 1H-Indol-4-ol, 5-methyl-can be achieved through multiple routes. One common method is synthesis by the reaction of p-methylaniline and acetylacetone. First, methylaniline reacts with acetylacetone to produce N-methyl -1-aniline-2-propanone. Then, the intermediate is oxidized and cyclized under the action of base to generate 1H-Indol-4-ol, 5-methyl-.
There is no clear record of toxicity or danger regarding the safety of 1H-Indol-4-ol, 5-methyl. However, as a chemical substance, care should be taken to comply with the safety procedures of chemical laboratories, including wearing appropriate protective equipment, avoiding contact with skin and eyes, and avoid inhalation or ingestion of the substance. In the case of accidental exposure or ingestion, medical assistance should be sought immediately. In addition, the compound should be stored in a dry, well-ventilated place, away from ignition and flammable materials.
The main use of this compound is as an intermediate in organic synthesis. It can be used to synthesize various similar compounds, such as fluorescent dyes, drugs, natural products, etc.
The preparation method of 1H-Indol-4-ol, 5-methyl-can be achieved through multiple routes. One common method is synthesis by the reaction of p-methylaniline and acetylacetone. First, methylaniline reacts with acetylacetone to produce N-methyl -1-aniline-2-propanone. Then, the intermediate is oxidized and cyclized under the action of base to generate 1H-Indol-4-ol, 5-methyl-.
There is no clear record of toxicity or danger regarding the safety of 1H-Indol-4-ol, 5-methyl. However, as a chemical substance, care should be taken to comply with the safety procedures of chemical laboratories, including wearing appropriate protective equipment, avoiding contact with skin and eyes, and avoid inhalation or ingestion of the substance. In the case of accidental exposure or ingestion, medical assistance should be sought immediately. In addition, the compound should be stored in a dry, well-ventilated place, away from ignition and flammable materials.
Last Update：2024-04-09 21:54:55
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CAS: 19499-83-3
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