(4-Chloro-2-isopropoxyphenyl)boronic acid
(4-Chloro-2-isopropoxyphenyl)boronic acid
CAS: 1256355-04-0
Molecular Formula: C9H12BClO3
(4-Chloro-2-isopropoxyphenyl)boronic acid - Names and Identifiers
(4-Chloro-2-isopropoxyphenyl)boronic acid - Physico-chemical Properties
| Molecular Formula | C9H12BClO3 |
| Molar Mass | 214.45 |
| Storage Condition | Sealed in dry,2-8°C |
| Sensitive | Irritant |
| MDL | MFCD17015770 |
(4-Chloro-2-isopropoxyphenyl)boronic acid - Introduction
boronic acid is an organic boron compound with the chemical formula C10H13BClO3, which is a white solid.
Nature:
boronic acid is soluble in organic solvents such as methanol, ethanol and dichloromethane, and slightly soluble in water. It is a stable compound, but decomposes under strong alkaline conditions.
Use:
(br) boronic acid is a reagent commonly used in organic synthesis, which can be used to synthesize heterocyclic compounds, fluorescent dyes and drug molecules. It can be used as a chelating agent, catalyst, ligand, etc. to participate in a series of chemical reactions.
Preparation Method:
(Br) boronic acid can be prepared by the reaction of phenylboronic acid and 3-chloropropanol. Specific synthetic methods can be found in the chemical literature.
Safety Information:
() boronic acid need to pay attention to safety when using. Avoid inhaling, chewing or swallowing, and avoid contact with skin and eyes. Wear appropriate protective equipment such as lab gloves, safety glasses, and lab coats during operation. Care should be taken to avoid producing harmful gases when reacting with other chemicals. In case of accidental contact, rinse immediately with plenty of water and seek medical help.
Nature:
boronic acid is soluble in organic solvents such as methanol, ethanol and dichloromethane, and slightly soluble in water. It is a stable compound, but decomposes under strong alkaline conditions.
Use:
(br) boronic acid is a reagent commonly used in organic synthesis, which can be used to synthesize heterocyclic compounds, fluorescent dyes and drug molecules. It can be used as a chelating agent, catalyst, ligand, etc. to participate in a series of chemical reactions.
Preparation Method:
(Br) boronic acid can be prepared by the reaction of phenylboronic acid and 3-chloropropanol. Specific synthetic methods can be found in the chemical literature.
Safety Information:
() boronic acid need to pay attention to safety when using. Avoid inhaling, chewing or swallowing, and avoid contact with skin and eyes. Wear appropriate protective equipment such as lab gloves, safety glasses, and lab coats during operation. Care should be taken to avoid producing harmful gases when reacting with other chemicals. In case of accidental contact, rinse immediately with plenty of water and seek medical help.
Last Update：2024-04-09 19:06:02
Supplier List
View History
(4-Chloro-2-isopropoxyphenyl)boronic acid
84434-67-3
1(2H)-Pyrimidineacetamide, N-[4-[[2-(2,6-dimethylphenoxy)acetyl]amino]-3-hydroxy-5-phenyl-1-(phenylmethyl)pentyl]tetrahydro-α-(1-methylpropyl)-2-oxo-
3-Quinolinecarboxylicacid, 4-chloro-6-fluoro-, ethyl ester
6-(tert-butoxycarbonyl)-6-azaspiro 2.5 octane-1-carboxylic acid(SALTDATA
84434-67-3
1(2H)-Pyrimidineacetamide, N-[4-[[2-(2,6-dimethylphenoxy)acetyl]amino]-3-hydroxy-5-phenyl-1-(phenylmethyl)pentyl]tetrahydro-α-(1-methylpropyl)-2-oxo-
3-Quinolinecarboxylicacid, 4-chloro-6-fluoro-, ethyl ester
6-(tert-butoxycarbonyl)-6-azaspiro 2.5 octane-1-carboxylic acid(SALTDATA