2,6-Dimethyl-pyridine-4-boronic acid

2,6-Dimethyl-pyridine-4-boronic acid - Names and Identifiers

Name	2,6-Dimethyl-pyridine-4-boronic acid
Synonyms	(2,6-Dimethylpyridin-4-yl) 2,6-Dimethylpyridin-4-boronic acid 2,6-Dimethylpyridine-4-boronic acid 2,6-Dimethyl-pyridine-4-boronic acid 2,6-dimethylpyridin-4-ylboronic acid 6-diMethylpyridin-4-yl-4-boronic acid (2,6-DiMethylpyridin-4-yl)boronic acid (2,6-Dimethylpyridin-4-yl)boronic acid 2,6-diMethylpyridin-4-yl-4-boronic acid B-(2,6-dimethyl-4-pyridinyl)-Boronic acid Boronic acid, B-(2,6-dimethyl-4-pyridinyl)- Carbamodithioic acid, (5-methoxy-3-pyridinyl)- (9ci)
CAS	846548-44-5
EINECS	200-528-9

2,6-Dimethyl-pyridine-4-boronic acid - Physico-chemical Properties

Molecular Formula	C7H10BNO2
Molar Mass	150.97
Density	1.14±0.1 g/cm3(Predicted)
Boling Point	316.9±52.0 °C(Predicted)
pKa	7.72±0.11(Predicted)
Storage Condition	Inert atmosphere,Store in freezer, under -20°C

2,6-Dimethyl-pyridine-4-boronic acid - Introduction

2, a kind of organic compound, chemical formula is C7H10BNO2. The following is a description of its nature, use, formulation and safety information:

Nature:
-Appearance: 2, acid is a white to light yellow crystalline solid.
-Solubility: Slightly soluble in water, soluble in organic solvents such as methanol and dimethylformamide.
-Melting point: about 150-155 degrees Celsius.
-Stable nature: stable at room temperature.

Use:
- 2, acid is an important reagent in the field of organic synthesis, commonly used in metal catalytic reactions, Cross-coupling (cross-coupling) reactions and reactions in organic synthesis.
-It can be used as a ligand in coordination chemistry to catalyze the formation of organometallic compounds, such as palladium and platinum complexes.
- 2, acid can also be used to prepare functional compounds, such as fluorescent dyes, heterocyclic compounds, etc.

Preparation Method: The preparation of
- 2, acid is generally obtained by reacting boric acid with 2,6-lutidine.
-The reaction often uses solvents such as methanol, chlorinated hydrocarbons or ethers, and usually requires extraction or crystallization purification after heating the reaction mixture to obtain the pure product.

Safety Information:
- 2, acid toxicity is low, but still need to be cautious.
-Wear appropriate personal protective equipment, such as lab gloves and goggles, to avoid inhalation, ingestion or contact with skin.
-Operate under airtight ventilation conditions to avoid release into the environment and avoid contact with oxidants and acidic substances.

Last Update：2024-04-10 22:29:15