3-Chloro-5-fluorophenylboronic acid
3-Chloro-5-fluorophenylboronic acid Basic information
- Product Name:
- 3-Chloro-5-fluorophenylboronic acid
- Synonyms:
-
- 3-Chloro-5-fluorobenzeneboronic acid ,98%
- 3-Chloro-5-fluorobenzeneboroni
- REF DUPL: 3-Chloro-5-fluorophenylboronic acid
- 3-CHLORO-5-FLUOROPHENYLBORONIC ACID
- 3-CHLORO-5-FLUOROBENZENEBORONIC ACID
- AKOS BRN-0721
- 3-Chloro-5-fluorobenzeneboronic acid 97%
- 3-Chloro-5-fluorobenzeneboronicacid97%
- CAS:
- 328956-61-2
- MF:
- C6H5BClFO2
- MW:
- 174.37
- Product Categories:
-
- blocks
- BoronicAcids
- FluoroCompounds
- Boronic Acids
- Mol File:
- 328956-61-2.mol
3-Chloro-5-fluorophenylboronic acid Chemical Properties
- Melting point:
- >200°C
- Boiling point:
- 308.1±52.0 °C(Predicted)
- Density
- 1.41±0.1 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- solubility
- soluble in Methanol
- form
- powder to crystal
- pka
- 6.52±0.10(Predicted)
- color
- White to Almost white
- Water Solubility
- Slightly soluble in water.
- CAS DataBase Reference
- 328956-61-2(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi,Xn
- Risk Statements
- 22-36/37/38
- Safety Statements
- 26-36
- HazardClass
- IRRITANT
- HS Code
- 29163990
3-Chloro-5-fluorophenylboronic acid Usage And Synthesis
Chemical Properties
White solid
Uses
3-Chloro-5-fluorobenzeneboronic acid is used as an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff.
Uses
suzuki reaction
Synthesis
121-43-7
33863-76-2
328956-61-2
Grignard's reagent was prepared by dissolving 11.3 g of dried magnesium shavings and 75.0 g of 1-bromo-3-chloro-5-fluorobenzene (S1-1) in 220 ml of anhydrous tetrahydrofuran (THF) under nitrogen protection. The reaction system was cooled to -70 °C and 52.0 g of trimethyl borate dissolved in 200 ml of THF was slowly added dropwise. The reaction temperature of -70°C was maintained and stirred for 3 hours. Subsequently, the reaction system was gradually warmed to room temperature and stirring was continued for 12 hours. Upon completion of the reaction, 2N hydrochloric acid was slowly added dropwise to the reaction solution and stirred for 1 hour. The reaction mixture was extracted with ethyl acetate, the organic phase was washed with water and dried over anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure and the residue was washed with heptane to give 34.7 g of 3-chloro-5-fluorophenylboronic acid (S1-2) in 55.7% yield.
References
[1] Patent: EP2433923, 2012, A1. Location in patent: Page/Page column 68
3-Chloro-5-fluorophenylboronic acid Preparation Products And Raw materials
Raw materials
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3-Chloro-5-fluorophenylboronic acid(328956-61-2)Related Product Information
- Phenylboronic acid
- 4-Fluorobenzeneboronic acid
- 4-Fluorobenzaldehyde
- Transfluthrin
- EPA
- Florfenicol
- Citric acid
- Ascoric Acid
- FENFLURAMINE
- 5-CHLORO-2-FLUOROPHENYLBORONIC ACID
- 6-Bromo-3-chloro-2-fluorophenylboronic acid
- 5-Bromo-3-chloro-2-fluorophenylboronic acid
- 3-(Benzyloxy)-2-chloro-6-fluorophenylboronic acid,3-Benzyloxy-2-chloro-6-fluorophenylboronic acid
- Difluorochloromethane
- 2-CHLORO-6-FLUOROPHENYLBORONIC ACID
- 4-CHLORO-2-FLUOROPHENYLBORONIC ACID
- 3-CHLORO-4-FLUOROPHENYLBORONIC ACID,3-Chloro-4-fluorophenylboronic Acid (contains varying amounts of Anhydride)
- 2-CHLORO-5-FLUOROPHENYLBORONIC ACID