3-Carboxy-4-chL

3-Carboxy-4-chL - Names and Identifiers

Name	2-chloro-5-(dihydroxyboranyl)benzoic acid
Synonyms	3-Carboxy-4-chL 5-Borono-2-chlorobenzoicaci 5-Borono-2-chlorobenzoicacid 3-Carboxy-4-chlorophenylboronic Benzoicacid, 5-borono-2-chloro- benzoic acid, 5-borono-2-chloro- 3-Carboxy-4-Chlorobenzeneboronic Acid 2-Chloro-5-(dihydroxyboryl)benzoic acid 2-chloro-5-(dihydroxyboranyl)benzoic acid 3-Carboxy-4-chlorophenylboronic Acid (contains varying amounts of Anhydride)
CAS	913835-32-2
InChI	InChI=1/C7H6BClO4/c9-6-2-1-4(8(12)13)3-5(6)7(10)11/h1-3,12-13H,(H,10,11)

3-Carboxy-4-chL - Physico-chemical Properties

Molecular Formula	C7H6BClO4
Molar Mass	200.38
Density	1.55±0.1 g/cm3(Predicted)
Melting Point	223-225
Boling Point	438.0±55.0 °C(Predicted)
Flash Point	218.71°C
Vapor Presure	0mmHg at 25°C
pKa	2.91±0.25(Predicted)
Storage Condition	Inert atmosphere,2-8°C
Refractive Index	1.604

3-Carboxy-4-chL - Risk and Safety

Hazard Symbols	Xi - Irritant
Hazard Note	Irritant/Keep Cold
Hazard Class	IRRITANT, KEEP COLD

3-Carboxy-4-chL - Introduction

2-chloro-5-(dihydroxyboranyl)benzoic acid is an organic compound with the chemical formula C7H6BClO4, and its structure contains a carboxyl group and a chlorine atom, and a borate group. The following is a description of its nature, use, preparation and safety information:

Nature:
1. Appearance: colorless crystalline or white powdery solid.
2. Melting point: about 180-185 degrees Celsius.
3. solubility: can be partially dissolved in water.

Use:
1.2-chroo-5-(dihydroxyboranyl)benzoic acid can be used as an important reagent in organic synthesis and is used to construct oxygen-containing and boron-containing compounds.
2. It can also be used to prepare other organic lithium compounds, organic metal complexes and catalysts.

Method:
A common preparation method is synthesized by the reaction of 4-chlorobenzeneboronic acid with iodic acid (iodic acid), the specific steps are as follows:
1. 4-Chlorobenzeneboronic acid is reacted with iodic acid in the presence of dilute sulfuric acid.
2. the product produced by the reaction is extracted and crystallized to obtain 2-chroo-5-(dihydroxyboranyl)benzoic acid.

Safety Information:
1.2-chroo-5-(dihydroxyboranyl)benzoic acid is a relatively safe compound under standard operating conditions.
2. in the operation, attention should be paid to avoid contact with eyes, skin and taking. In case of contact, rinse with plenty of water and seek medical help.
3. During storage, it is necessary to keep dry and sealed to avoid contact with oxidants and other substances.

Last Update：2024-04-10 22:29:15