2-Isopropylphebylboronic acid - Names and Identifiers
2-Isopropylphebylboronic acid - Physico-chemical Properties
Molecular Formula | C9H13BO2
|
Molar Mass | 164.01 |
Density | 1.04±0.1 g/cm3(Predicted) |
Melting Point | 85-86°C |
Boling Point | 297.2±33.0 °C(Predicted) |
Flash Point | 133.5°C |
Vapor Presure | 0.000616mmHg at 25°C |
Appearance | White-like crystal |
BRN | 3090298 |
pKa | 8.63±0.58(Predicted) |
Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
Refractive Index | 1.513 |
MDL | MFCD03411937 |
2-Isopropylphebylboronic acid - Risk and Safety
Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin.
R36 - Irritating to the eyes
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.
S36 - Wear suitable protective clothing.
|
HS Code | 29319090 |
Hazard Class | IRRITANT |
2-Isopropylphebylboronic acid - Introduction
(2-Isoppylphenyl) boronic acid is an organic compound with the chemical formula C9H13BO2. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: White crystalline solid.
-Solubility: Soluble in organic solvents such as ethanol, dimethyl amide and dichloromethane, slightly soluble in water.
-Melting point: about 73-77°C.
-Stability: relatively stable under dry conditions, but may be damp in a humid environment.
Use:
- (2-Isopropylphenyl)boronic acid is an important organic boron compound, which has a wide range of applications in organic synthesis.
-It can be used as a ligand or reagent to participate in metal-catalyzed reactions, such as Suzuki-Miyaura coupling reactions.
-In the field of medicine, it can be used to synthesize drug intermediates and biologically active molecules, such as drugs, anti-tumor substances, etc.
Preparation Method:
- (2-Isopropylphenyl)boronic acid is generally obtained by reacting phenylboronic acid with 2-isopropyl phenol. The reaction is usually carried out under an inert atmosphere, and a solvent such as ethanol or methanol can be selected.
-The control of reaction temperature and time has an important effect on yield and purity.
Safety Information:
- (2-Isopropylphenyl)boronic acid may have an irritating effect on the skin, eyes and respiratory system. Immediately after contact, rinse with water for a large amount of time. Avoid inhalation and ingestion.
-During use and storage, avoid ignition and avoid contact with strong oxidants.
-Please refer to the Safety Data Sheet (MSDS) of the chemical for more detailed safety information.
Last Update:2024-04-09 02:00:49