328-73-4
3,5-Bis(Trifluoromethyl) Iodobenzene
CAS: 328-73-4
Molecular Formula: C8H3F6I
328-73-4 - Names and Identifiers
328-73-4 - Physico-chemical Properties
| Molecular Formula | C8H3F6I |
| Molar Mass | 340 |
| Density | 1.919 g/mL at 25 °C (lit.) |
| Boling Point | 59-61 °C/10 mmHg (lit.) |
| Flash Point | 166°F |
| Water Solubility | Slightly soluble in water. |
| Vapor Presure | 1.03mmHg at 25°C |
| Appearance | Liquid |
| Color | White or Colorless to Light yellow |
| BRN | 2461627 |
| Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
| Sensitive | Light Sensitive |
| Refractive Index | n20/D 1.463(lit.) |
| Physical and Chemical Properties | Light pink liquid |
328-73-4 - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. |
| WGK Germany | 3 |
| HS Code | 29039990 |
| Hazard Note | Irritant/Light sensitive |
| Hazard Class | IRRITANT |
328-73-4 - Introduction
3,5-bis (Trifluoromethyl) Iodobenzene is an organic compound with the chemical formula C8H3F6I. It is a colorless solid with a low boiling point and melting point.
3,5-bis (Trifluoromethyl) Iodobenzene is a commonly used reagent and reactant in organic synthesis. One of its main uses is as a fluorinating reagent, which can be used to introduce trifluoromethyl groups. In addition, it can also be used as an oxidizing agent, a transition metal ligand, etc.
The common method for preparing 3,5-bis (Trifluoromethyl) Iodobenzene is obtained by reacting Iodobenzene with trifluoroacetic acid and Nitro camphor. Specific reaction processes and operating conditions can be found in organic chemistry textbooks or literature.
Since 3,5-bis (Trifluoromethyl) Iodobenzene is a chemical, safety precautions should be paid attention to when using it. It may cause irritation and damage to the skin, eyes and respiratory system, so care should be taken to wear appropriate personal protective equipment, such as gloves, goggles and protective masks. At the same time, avoid contact with combustibles during storage and handling, and ensure that it is used in a well-ventilated place. Detailed safety information can be found in the safety data sheet (SDS) of the chemical. Most importantly, you must follow the laboratory procedures and use it in the right way.
3,5-bis (Trifluoromethyl) Iodobenzene is a commonly used reagent and reactant in organic synthesis. One of its main uses is as a fluorinating reagent, which can be used to introduce trifluoromethyl groups. In addition, it can also be used as an oxidizing agent, a transition metal ligand, etc.
The common method for preparing 3,5-bis (Trifluoromethyl) Iodobenzene is obtained by reacting Iodobenzene with trifluoroacetic acid and Nitro camphor. Specific reaction processes and operating conditions can be found in organic chemistry textbooks or literature.
Since 3,5-bis (Trifluoromethyl) Iodobenzene is a chemical, safety precautions should be paid attention to when using it. It may cause irritation and damage to the skin, eyes and respiratory system, so care should be taken to wear appropriate personal protective equipment, such as gloves, goggles and protective masks. At the same time, avoid contact with combustibles during storage and handling, and ensure that it is used in a well-ventilated place. Detailed safety information can be found in the safety data sheet (SDS) of the chemical. Most importantly, you must follow the laboratory procedures and use it in the right way.
Last Update：2024-04-10 22:29:15
