3-(Bromoacetyl)benzothiophene - Names and Identifiers
3-(Bromoacetyl)benzothiophene - Physico-chemical Properties
Molecular Formula | C10H7BrOS
|
Molar Mass | 255.13 |
Density | 1.617g/cm3 |
Melting Point | 138 °C |
Boling Point | 352°C at 760 mmHg |
Flash Point | 166.7°C |
Vapor Presure | 3.96E-05mmHg at 25°C |
Storage Condition | under inert gas (nitrogen or Argon) at 2–8 °C |
Refractive Index | 1.689 |
3-(Bromoacetyl)benzothiophene - Risk and Safety
Hazard Symbols | C - Corrosive
|
Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin.
R34 - Causes burns
|
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.
S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S26/37/39 -
|
UN IDs | 3261 |
HS Code | 29349990 |
Hazard Note | Corrosive |
Hazard Class | IRRITANT |
3-(Bromoacetyl)benzothiophene - Introduction
1-benzo [B] thiophen-3-yl-2-bromoethan-1-one is an organic compound with the chemical formula C12H8BrOS. The following is a detailed description of the properties, uses, preparation and safety information of the compound:
Nature:
-Appearance: 1-benzo [B] thiophen-3-yl-2-bromoethan-1-one is a solid substance, showing white to light yellow crystal particles at room temperature.
-Melting point: The melting point of the compound is about 80-82 degrees Celsius.
-Solubility: It has certain solubility in some organic solvents such as ethanol, dimethyl sulfoxide and chloroform.
Use:
1-benzo [B] thiophen-3-yl-2-bromoethan-1-one are commonly used in organic synthesis reactions and can be used as important intermediates or reagents. It has a wide range of applications in drug synthesis, natural product synthesis and organic chemical reactions.
Method:
1-benzo [B] thiophen-3-yl-2-bromoethan-1-one can be synthesized by the following steps:
1. 1-benzo [B] thiophene and bromoacetic acid are reacted to obtain 1-benzo [B] thiophen-3-yl-2-bromoacetic acid.
2. 1-benzo [B] thiophen-3-yl-2-bromoacetic acid is converted into 1-benzo [B] thiophen-3-yl-2-bromoethan-1-one by reacting with sodium carbonate under alkaline conditions.
Safety Information:
-Since there is no specific safety information to provide, when using chemicals, be sure to follow the correct laboratory operating procedures and wear appropriate personal protective equipment, avoid direct contact with skin and eyes, and use in a well-ventilated area.
Last Update:2024-04-09 21:04:16