2,4,6-Tribromothiophenol - Names and Identifiers
Name | 2,4,6-Tribromothiophenol
|
Synonyms | 2,4,6-Tribromothioph 2,4,6-tribromothiophenol 2,4,6-Tribromothiophenol 2,4,6-Tribromobenzenethiol Benzenethiol, 2,4,6-tribromo- BENZENETHIOL 2,4,6-TRIBROMINE Benzenethiol 2,4,6-tribromine
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CAS | 57730-98-0
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InChI | InChI=1/C6H3Br3S/c7-3-1-4(8)6(10)5(9)2-3/h1-2,10H |
2,4,6-Tribromothiophenol - Physico-chemical Properties
Molecular Formula | C6H3Br3S
|
Molar Mass | 346.86 |
Density | 2.303±0.06 g/cm3(Predicted) |
Melting Point | 115.5-115.9 °C |
Boling Point | 328.8±42.0 °C(Predicted) |
Flash Point | 152.7°C |
Vapor Presure | 0.000354mmHg at 25°C |
pKa | 4.63±0.50(Predicted) |
Refractive Index | 1.689 |
2,4,6-Tribromothiophenol - Introduction
2,4,6-Tribromothiophenol is an organic compound with the formula C6H2Br3SH. The following is a description of its nature, use, preparation and safety information:
Nature:
2,4,6-Tribromothiophenol is an organic compound with a benzene ring and a thiophenol group. It is a light yellow solid, crystalline at room temperature, soluble in organic solvents. The compound has a high melting point and boiling point, and has a strong odor.
Use:
2,4,6-Tribromothiophenol is widely used in chemical research and laboratories. It can be used as an important intermediate for the synthesis of drugs, dyes and pesticides and other organic compounds. In addition, it can also be used as a reagent and oxidant for spectral analysis.
Preparation Method:
2,4,6-Tribromothiophenol is usually synthesized by substituting the halogen on the benzene ring. First, a hydrogen atom on the benzene ring is substituted with bromine to give a bromophenol. Sulfur is then added as an electrophile to introduce a thiophenol group into the compound to form 2,4,6-Tribromothiophenol.
Safety Information:
2,4,6-Tribromothiophenol needs to be safe during use and storage. It is an irritating chemical that can cause irritation and damage to the eyes, skin and respiratory tract. Therefore, when operating, you should wear appropriate personal protective equipment to avoid direct contact. In addition, the operation should be carried out in a well-ventilated place to avoid inhaling harmful gases. For any inadvertent contact, rinse immediately with plenty of water and seek medical help. When storing, it should be kept in a dry, cool, ventilated place, away from fire and oxidant.
Last Update:2024-04-09 21:01:54