871125-86-9

871125-86-9 - Names and Identifiers

Name	1-(5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PYRIDIN-2-YL)PIPERAZINE
Synonyms	2-piperazinyl pyridine-5-boronic acid 2-Piperazinopyridine-5-boronic acid, pinacol ester 6-PIPERAZINYLPYRIDINE-3-BORONIC ACID, PINACOL ESTER 6-PIPERAZIN-1-YL-PYRIDINE-3-BORONIC ACID, PINACOL ESTER 2-(PIPERAZIN-1-YL)PYRIDINE-5-BORONIC ACID, PINACOL ESTER 1-[5-(tetraMethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]piperazine 1-(5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PYRIDIN-2-YL)PIPERAZINE
CAS	871125-86-9

871125-86-9 - Physico-chemical Properties

Molecular Formula	C15H24BN3O2
Molar Mass	289.18
Melting Point	137-142 °C
Appearance	Powder
Color	White to off-white
Storage Condition	2-8℃

871125-86-9 - Risk and Safety

Hazard Symbols	Xi - Irritant
Risk Codes	36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description	S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing.
WGK Germany	3
HS Code	29335995

871125-86-9 - Upstream Downstream Industry

Downstream Products

S)-1-(sec-butyl)-N-((4,6-diMethyl-2-oxo-1,2-dihydropyridin-3-yl)Methyl)-3-Methyl-6-(6-(piperazin-1-yl)pyridin-3-yl)-1H-indole-4-carboxaMide

871125-86-9 - Introduction

1-(5-(4,4, 5,5-tetramethyl-1, 3,2-dioxaborolan-2-yl) PYRIDIN-2-YL)PIPERAZINE is an organic compound whose chemical structure contains PIPERAZINE and pyridine rings, and there is a pinacol borate ester group attached.

The properties of the compound are as follows:
-Appearance: Usually a white crystalline solid.
-Molecular formula: C15H24BN3O2
-Molecular weight: 293.18g/mol

1-(5-(4,4, 5,5-tetramethyl-1, 3,2-dioxaborolan-2-yl) PYRIDIN-2-YL)PIPERAZINE is mainly used as a ligand or reaction reagent in the field of organic synthesis. It is commonly used in Suzuki coupling reactions, catalytic reduction and catalytic oxidation reactions. In addition, it is used as an intermediate in pharmaceutical research.

The preparation method, 1-(5-(4,4, 5,5-tetramethyl-1, 3,2-dioxaborolan-2-yl) PYRIDIN-2-YL)PIPERAZINE can be obtained by reacting PIPERAZINE -1-ethanol with pyridine-5-boronic acid. The use of appropriate solvents and reaction conditions during the reaction results in high yields of product.

With regard to safety information, specific data on this compound may be limited, so use is subject to relevant laboratory safety procedures. In general, organic compounds are potentially harmful to the human body, so contact with the skin and inhalation of its particles should be avoided during handling and storage. If necessary, wear suitable personal protective equipment such as protective glasses and gloves.

Last Update：2024-04-09 21:48:26