3-(N-Ethylaminocarbonyl)Benzeneboronic Acid

3-(N-Ethylaminocarbonyl)Benzeneboronic Acid - Names and Identifiers

Name	[3-(ethylcarbamoyl)phenyl]boronic acid
Synonyms	3-(Ethylcarbamoyl)benzeneboronic acid [3-(ethylcarbamoyl)phenyl]boronic acid [3-(Ethylcarbamoyl)phenyl]boronic acid 3-(N-Ethylaminocarbonyl)phenylboronicacid 3-(N-ETHYLAMINOCARBOYL)PHENYLBORONIC ACID 3-(N-Ethylaminocarbonyl)Benzeneboronic Acid Boronic acid,B-[3-[(ethylaMino)carbonyl]phenyl]- boronic acid, B-[3-[(ethylamino)carbonyl]phenyl]- BORONICACID, [3-[(ETHYLAMINO)CARBONYL]PHENYL]- (9CI) Boronicacid, [3-[(ethylamino)carbonyl]phenyl]- (9CI) 3-[(Ethylamino)carbonyl]benzeneboronic acid, 3-Borono-N-ethylbenzamide 3-(Ethylcarbamoyl)benzeneboronic acid(contains varying amounts of Anhydride)
CAS	850567-21-4
InChI	InChI=1/C9H12BNO3/c1-2-11-9(12)7-4-3-5-8(6-7)10(13)14/h3-6,13-14H,2H2,1H3,(H,11,12)

3-(N-Ethylaminocarbonyl)Benzeneboronic Acid - Physico-chemical Properties

Molecular Formula	C9H12BNO3
Molar Mass	193.01
Density	1.19±0.1 g/cm3(Predicted)
Melting Point	106-116°C
pKa	7.95±0.10(Predicted)
Storage Condition	2-8°C
Refractive Index	1.545

3-(N-Ethylaminocarbonyl)Benzeneboronic Acid - 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. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
Hazard Note	Irritant

3-(N-Ethylaminocarbonyl)Benzeneboronic Acid - Introduction

[3-(ethylcarbamoyl)phenyl]boronic acid is an organic compound with the chemical formula C10H14BNO3.

Its properties are as follows:
-Appearance: White crystalline solid
-Melting point: about 120-124 degrees Celsius
-Solubility: Soluble in general organic solvents, such as ether, chloroform and dichloromethane, insoluble in water

[3-(ethylcarbamoyl)phenyl] The main uses of boronic acid are as follows:
-As an important intermediate in organic synthesis, it can be used to synthesize various functional compounds, such as drugs, pesticides and optical materials.
-In the pharmaceutical field, it can be used to synthesize anticancer drugs, antiviral drugs and biomarkers.
-In chemical research, catalysts and ligands that can be used in organic reactions.

[3-(ethylcarbamoyl)phenyl] The preparation method of boronic acid mainly includes the following steps:
1. the reaction of phenylboronic acid and ethanolamine to generate N-ethyl formylamino phenyl borate.
2. react n-ethyl formylaminophenyl borate with hydrochloric acid to remove amine to generate [3-(ethylcarbamoyl)phenyl]boronic acid.

During operation, attention should be paid to the safe use of [3-(ethylcarbamoyl)phenyl]boronic acid and avoid contact with skin, eyes and respiratory tract. During storage, it should be kept away from heat and fire sources, and stored in a sealed container to avoid contact with oxidants and strong acids.

Last Update：2024-04-09 02:00:48