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2-Chloropyrimidine-5-Boronic Acid CAS 1003845-06-4

2-Chloropyrimidine-5-Boronic Acid - Names and IdentifiersName2-Chloropyrimidine-5-Boronic AcidS

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2-Chloropyrimidine-5-Boronic Acid - Names and Identifiers

Name2-Chloropyrimidine-5-Boronic Acid
Synonyms2-Chloropyrimidine-5-boro...
2-Chloro-pyridineyl-5-boronic
2-Chloro-5-pyrimidineboronicacid
2-CHLORO-5-PYRIMIDINEBORONIC ACID
2-Chloro-5-pyrimidineboronic acid
2-CHLOROPYRIMIDIN-5-YLBORONICACID
2-CHLOROPYRIMIDINE-5-BORONIC ACID
2-Chloropyrimidine-5-Boronic Acid
2-Chloro-pyridineyl-5-boronic acid
2-chloropyrimidin-5-ylboronic acid
BORONIC ACID,B-(2-CHLORO-5-PYRIMIDINYL)-
2-ChloropyriMidine-5-boronic acid (contains varying aMounts of anhydride)
CAS1003845-06-4
InChIInChI=1/C4H4BClN2O2/c6-4-7-1-3(2-8-4)5(9)10/h1-2,9-10H

2-Chloropyrimidine-5-Boronic Acid - Physico-chemical Properties

Molecular FormulaC4H4BClN2O2
Molarmassa158.35
Täthet1.52±0.1 g/cm3(Predicted)
Boling Point425.4±37.0 °C(Predicted)
UtseendePowder
FärgVit
pKa5.03±0.11(Predicted)
Lagringstillståndunder inert gas (nitrogen or Argon) at 2–8 °C
MDLMFCD08063113

2-Chloropyrimidine-5-Boronic Acid - Introduction

2-chloropyrimidine-5-boronic acid (acid) is an organic compound with the chemical formula C4H4BClN2O2.

Nature:
2-chloropyrimidine-5-boronic acid is a colorless solid and can be dissolved in some organic solvents such as dimethyl sulfoxide, dichloromethane, etc. It is an important boric acid compound with high chemical stability.

Use:
2-chloropyrimidine-5-boronic acid is commonly used in organic synthesis as an organic heavy raw material, which can be used to synthesize compounds with important physiological activities. Among them, 2-chloropyrimidine group can undergo Suzuki coupling reaction and react with compounds containing active aryl groups to synthesize various derivatives, which are commonly used in drug synthesis, pesticide synthesis and other organic synthesis fields.

Preparation Method:
The preparation of 2-chloropyrimidine-5-boronic acid is often carried out by reacting 2-chloropyrimidine and boric acid. In general, 2-chloropyrimidine is first reacted with an alkaline substrate (e. g., sodium carbonate) to form the corresponding negative halide ion, which is then reacted with boric acid to give the desired product.

Safety Information:
2-chloropyrimidine -5-boric acid has a certain irritating effect on the eyes, skin and respiratory system. Wear suitable protective gloves, goggles and breathing apparatus to avoid contact with and inhalation of the compound during operation. During storage, keep away from heat sources, fire sources and oxidants to avoid fire or explosion.

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