959972-40-8
2-(4-(2-Methoxyethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS: 959972-40-8
Molecular Formula: C15H23BO4
959972-40-8 - Names and Identifiers
| Name | 2-(4-(2-Methoxyethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane |
| Synonyms | 2-(4-(2-Methoxyethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane |
| CAS | 959972-40-8 |
959972-40-8 - Physico-chemical Properties
| Molecular Formula | C15H23BO4 |
| Molar Mass | 278.15 |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD23143157 |
959972-40-8 - Introduction
2-(4-(2-Methoxyethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, also known as 2-(4-(2-Methoxyethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, is an organic boron compound.
Properties of the compound include:
-Molecular formula: C15H23BO3
-Molecular weight: 262.16g/mol
-Appearance: Colorless to light yellow oily liquid
-Melting Point: No specific melting point
-Boiling point: about 200-210 degrees Celsius
-Solubility: Soluble in common organic solvents such as ethanol and dimethylformamide
The main use of this compound is as a reagent for organic synthesis reactions, especially in metal-catalyzed C- C bond formation reactions. It can be used in conjunction with copper catalysts to participate in Suzuki-Miyaura cross-coupling reactions, C- H bond functionalization reactions, electrophilic substitution reactions, etc. In addition, there are applications in the pharmaceutical field for the synthesis of active molecules in drugs.
The method for preparing the compound can be obtained by reacting phenylboronic acid with 2-methoxyethanol to obtain the corresponding ester, and then converting it into the compound. The specific reaction steps may be carried out under appropriate conditions.
Regarding safety information, according to the safety requirements of chemicals, protective glasses and gloves should be worn during operation. Good laboratory practices should be followed and the compound should be stored and handled properly to avoid potential hazards. When using this compound, care should be taken to prevent contact with skin, eyes and inhalation. In case of contact, please rinse immediately with plenty of water and seek medical help. Detailed safety information and handling methods should refer to the relevant chemical safety manual or material safety data sheet (MSDS).
Properties of the compound include:
-Molecular formula: C15H23BO3
-Molecular weight: 262.16g/mol
-Appearance: Colorless to light yellow oily liquid
-Melting Point: No specific melting point
-Boiling point: about 200-210 degrees Celsius
-Solubility: Soluble in common organic solvents such as ethanol and dimethylformamide
The main use of this compound is as a reagent for organic synthesis reactions, especially in metal-catalyzed C- C bond formation reactions. It can be used in conjunction with copper catalysts to participate in Suzuki-Miyaura cross-coupling reactions, C- H bond functionalization reactions, electrophilic substitution reactions, etc. In addition, there are applications in the pharmaceutical field for the synthesis of active molecules in drugs.
The method for preparing the compound can be obtained by reacting phenylboronic acid with 2-methoxyethanol to obtain the corresponding ester, and then converting it into the compound. The specific reaction steps may be carried out under appropriate conditions.
Regarding safety information, according to the safety requirements of chemicals, protective glasses and gloves should be worn during operation. Good laboratory practices should be followed and the compound should be stored and handled properly to avoid potential hazards. When using this compound, care should be taken to prevent contact with skin, eyes and inhalation. In case of contact, please rinse immediately with plenty of water and seek medical help. Detailed safety information and handling methods should refer to the relevant chemical safety manual or material safety data sheet (MSDS).
Last Update：2024-04-09 20:02:46
