110851-66-6
3-Tetradecylthiophene
CAS: 110851-66-6
Molecular Formula: C18H32S
110851-66-6 - Names and Identifiers
| Name | 3-Tetradecylthiophene |
| Synonyms | 3-Tetradecylthiophene 3-n-Tetradecylthiophene thiophene, 3-tetradecyl- Thiophene, 3-tetradecyl- |
| CAS | 110851-66-6 |
| InChI | InChI=1/C18H32S/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-18-15-16-19-17-18/h15-17H,2-14H2,1H3 |
110851-66-6 - Physico-chemical Properties
| Molecular Formula | C18H32S |
| Molar Mass | 280.51 |
| Density | 0.9196 (estimate) |
| Melting Point | 14.85°C (estimate) |
| Boling Point | 348.22°C (estimate) |
| Flash Point | 129.9°C |
| Vapor Presure | 3.57E-05mmHg at 25°C |
| Maximum wavelength(λmax) | 244nm(CHCl3)(lit.) |
| Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
| Refractive Index | 1.4840 to 1.4880 |
| MDL | MFCD09750675 |
110851-66-6 - Introduction
3-Tetradecylthiophene is an organic compound with the chemical formula C14H30S. It is an organic sulfur compound with certain characteristics and applications.
In terms of nature, 3-tetradecylthiophene is a colorless or light yellow liquid with a strong odor. It has low solubility and is soluble in organic solvents such as ethanol and ether. In addition, the compound has high thermal and chemical stability.
In terms of application, 3-tetradecylthiophene is often used as a catalyst or ligand in organic synthesis reactions. It can help catalyze different chemical reactions in organic synthesis, such as cyclization, esterification and nucleophilic substitution reactions. In addition, 3-tetradecylthiophene is also used for the preparation of organic electronic devices and functional materials.
In terms of preparation method, 3-tetradecylthiophene can be obtained by condensation reaction of thiophene and corresponding 14-haloalkane. During the synthesis, it is necessary to use basic conditions and appropriate solvents to facilitate the reaction.
In terms of safety information, 3-tetradecylthiophene is relatively stable under general conditions of use, but it is still necessary to pay attention to safe operation. It has a pungent odor and should avoid excessive inhalation or contact with skin, eyes and mucous membranes. In the process of use, should wear protective glasses, gloves and appropriate protective clothing, and maintain good ventilation conditions. If exposed to the compound, rinse immediately with plenty of water and seek medical advice. Also, store, handle and dispose of in compliance with local regulations.
In terms of nature, 3-tetradecylthiophene is a colorless or light yellow liquid with a strong odor. It has low solubility and is soluble in organic solvents such as ethanol and ether. In addition, the compound has high thermal and chemical stability.
In terms of application, 3-tetradecylthiophene is often used as a catalyst or ligand in organic synthesis reactions. It can help catalyze different chemical reactions in organic synthesis, such as cyclization, esterification and nucleophilic substitution reactions. In addition, 3-tetradecylthiophene is also used for the preparation of organic electronic devices and functional materials.
In terms of preparation method, 3-tetradecylthiophene can be obtained by condensation reaction of thiophene and corresponding 14-haloalkane. During the synthesis, it is necessary to use basic conditions and appropriate solvents to facilitate the reaction.
In terms of safety information, 3-tetradecylthiophene is relatively stable under general conditions of use, but it is still necessary to pay attention to safe operation. It has a pungent odor and should avoid excessive inhalation or contact with skin, eyes and mucous membranes. In the process of use, should wear protective glasses, gloves and appropriate protective clothing, and maintain good ventilation conditions. If exposed to the compound, rinse immediately with plenty of water and seek medical advice. Also, store, handle and dispose of in compliance with local regulations.
Last Update：2024-04-10 22:30:50
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