4-Chloro-3-cyanophenylboronic acid, 4-Chloro-3-cyanobenzeneboronic acid - Names and Identifiers
4-Chloro-3-cyanophenylboronic acid, 4-Chloro-3-cyanobenzeneboronic acid - Physico-chemical Properties
Molecular Formula | C7H5BClNO2
|
Molar Mass | 181.38 |
Density | 1.41±0.1 g/cm3(Predicted) |
Melting Point | 300-304 |
Boling Point | 380.4±52.0 °C(Predicted) |
Flash Point | 183.9°C |
Vapor Presure | 1.83E-06mmHg at 25°C |
Appearance | Solid |
Color | White to yellow |
pKa | 6.98±0.10(Predicted) |
Storage Condition | Inert atmosphere,2-8°C |
Refractive Index | 1.58 |
MDL | MFCD08056360 |
4-Chloro-3-cyanophenylboronic acid, 4-Chloro-3-cyanobenzeneboronic acid - Risk and Safety
Hazard Symbols | Xi - Irritant
|
Risk Codes | R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed.
R36/37/38 - Irritating to eyes, respiratory system and skin.
R22 - Harmful if swallowed
|
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.
S60 - This material and its container must be disposed of as hazardous waste.
S36/37 - Wear suitable protective clothing and gloves.
|
UN IDs | 3439 |
HS Code | 29319090 |
Hazard Note | Irritant/Keep Cold |
Hazard Class | 6.1 |
Packing Group | Ⅲ |
4-Chloro-3-cyanophenylboronic acid, 4-Chloro-3-cyanobenzeneboronic acid - Introduction
Acid is an organic compound with the chemical formula C7H5BClNO2. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: acid is white crystalline powder.
-Melting point: about 170-175°C.
-Solubility: Soluble in common organic solvents such as chloroform, disulfide and dimethyl sulfoxide, slightly soluble in water.
Use:
-acid is an important organic synthesis intermediate, commonly used in organic synthesis reactions. It can be used as a synthetic reagent for aromatic compounds and their derivatives.
Preparation Method:
-and acid is usually prepared by the following steps:
1. First, 4-chloro -3-cyanoiodobenzene is reacted with sodium hydroxide to generate the corresponding phenolate compound.
2. Then, the phenolate is reacted with boric acid and a catalyst to form a phenol acid.
Safety Information:
-the specific toxicity information of acid may be limited, so it should be handled with caution during use.
-Avoid skin contact and eye contact to avoid irritation. In case of contact, rinse immediately with plenty of water.
-Wear appropriate protective equipment such as lab gloves, goggles and lab coats during operation.
-The operation should be carried out in a well-ventilated place to avoid inhaling the powder or the gas generated.
-Storage should be sealed and kept away from fire and oxidizing agents.
Please note that the information provided above is for reference only. Please follow relevant safety practices when using and handling chemicals.
Last Update:2024-04-10 22:29:15