4-AMINOCARBONYLPHENYLBORONIC ACID, PINACOL ESTER

4-AMINOCARBONYLPHENYLBORONIC ACID, PINACOL ESTER - Names and Identifiers

Name	4-AMINOCARBONYLPHENYLBORONIC ACID, PINACOL ESTER
Synonyms	4-(tetraMethyl-1,3,2-dioxaborolan-2-yl)benzaMide 4-AMINOCARBONYLPHENYLBORONIC ACID, PINACOL ESTER 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-BENZAMIDE Benzamide, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
CAS	179117-44-3

4-AMINOCARBONYLPHENYLBORONIC ACID, PINACOL ESTER - Physico-chemical Properties

Molecular Formula	C13H18BNO3
Molar Mass	247.098
Boling Point	388.2℃ at 760mmHg
Storage Condition	under inert gas (nitrogen or Argon) at 2-8°C

4-AMINOCARBONYLPHENYLBORONIC ACID, PINACOL ESTER - Risk and Safety

Hazard Symbols	Xn - Harmful
Risk Codes	22 - Harmful if swallowed
WGK Germany	3

4-AMINOCARBONYLPHENYLBORONIC ACID, PINACOL ESTER - Upstream Downstream Industry

Raw Materials	4-Carboxylphenylboronic acid pinacol ester 4-Chlorobenzamide 4-IODOBENZAMIDE 4-BROMOBENZAMIDE Pinacol 4-Bromobenzoic acid Pinacolborane Bis(pinacolato)diboron
Downstream Products	3-AMINOCARBONYLPHENYLBORONIC ACID, PINACOL ESTER

4-AMINOCARBONYLPHENYLBORONIC ACID, PINACOL ESTER - Introduction

ACID, Pinol ESTER, chemical formula C14H17BN2O3, is an organic compound. The following is a description of its nature, use, formulation and safety information:

1. Nature:
-Appearance: White crystalline powder or crystal.
-Melting point: About 150-154 ° C.
-Solubility: Soluble in some organic solvents, such as dimethyl sulfoxide (DMSO), dimethylformamide (DMF) and chloroform.

2. Use: -ACID, PINACOL ESTER is commonly used as a reagent and intermediate in organic synthesis.
-It can participate in Suzuki coupling reaction to generate aromatic compounds.
-It can also be used to construct heterocyclic compounds and intermediates for the synthesis of drugs.

3. Preparation method: -ACID, PINACOL ESTER is usually synthesized by chemical reaction.
-A commonly used method is to react 4-aminobenzamide with an esterification reagent of boric acid, such as 4-methyl -2-oxocyclohexanyl -2-butenyl ester (pinacol ester).
-The reaction is usually carried out under an inert atmosphere at room temperature or above room temperature, and is carried out under base catalysis.

4. Safety Information:
-the specific hazard and toxicity data of ACID, PINACOL ESTER may be limited, so appropriate safety measures and experimental operations should be carried out before use.
-Wear appropriate personal protective equipment such as chemical safety glasses, gloves and protective clothing when used.
-Avoid inhalation, contact with skin and eyes. If contact occurs, flush immediately with plenty of water and seek medical help.
-Should be stored in a dry, cool place, away from fire and oxidizing agents. Avoid contact with flammable substances and strong oxidants.

Please note that this information is for informational purposes only and it is recommended to refer to the exact Chemical Safety Data Sheet and to operate in a professional laboratory environment for specific use and operation.

Last Update：2024-04-09 20:49:11