7-(Methylsulfanyl)-1H-indole
1H-Indole, 7-(Methylthio)-
CAS: 936902-07-7
Molecular Formula: C9H9NS
7-(Methylsulfanyl)-1H-indole - Names and Identifiers
| Name | 1H-Indole, 7-(Methylthio)- |
| Synonyms | 7-(Methylthio)-1H-indole 1H-Indole, 7-(Methylthio)- 7-(Methylsulfanyl)-1H-indole |
| CAS | 936902-07-7 |
7-(Methylsulfanyl)-1H-indole - Physico-chemical Properties
| Molecular Formula | C9H9NS |
| Molar Mass | 163.24 |
| Boling Point | |
| Storage Condition | 2-8°C |
7-(Methylsulfanyl)-1H-indole - Introduction
1H-Indole, 7-(Methylthio)-is an organic compound with the chemical formula C9H9NS. It is a colorless to pale yellow crystalline solid with a strong ammonolysis and fishy odor.
1H-Indole, 7-(Methylthio)-is commonly used in organic synthesis as an important intermediate. It can play an important role in the synthesis of organic compounds such as hormones, drugs and pesticides. In addition, it can also be used as a fungicide, preservative and dye.
A common method for preparing 1H-Indole, 7-(Methylthio)-is by reacting 1H-indole with a thiomethyl compound. In this reaction, lH-indole is reacted with thiomethanol (usually a sulfide) under basic conditions to yield 1H-Indole, 7-(Methylthio)-.
Regarding safety information, 1H-Indole, 7-(Methylthio)-is compatible with most organic compounds at room temperature, but should avoid contact with strong oxidants and strong acids. Appropriate personal protective equipment such as gloves and goggles should be worn during operation. In addition, it should be kept away from fire and sparks. After exposure to or inhalation of the compound, rinse immediately with water and seek medical help.
1H-Indole, 7-(Methylthio)-is commonly used in organic synthesis as an important intermediate. It can play an important role in the synthesis of organic compounds such as hormones, drugs and pesticides. In addition, it can also be used as a fungicide, preservative and dye.
A common method for preparing 1H-Indole, 7-(Methylthio)-is by reacting 1H-indole with a thiomethyl compound. In this reaction, lH-indole is reacted with thiomethanol (usually a sulfide) under basic conditions to yield 1H-Indole, 7-(Methylthio)-.
Regarding safety information, 1H-Indole, 7-(Methylthio)-is compatible with most organic compounds at room temperature, but should avoid contact with strong oxidants and strong acids. Appropriate personal protective equipment such as gloves and goggles should be worn during operation. In addition, it should be kept away from fire and sparks. After exposure to or inhalation of the compound, rinse immediately with water and seek medical help.
Last Update：2024-04-09 20:52:54
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