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ChemicalBook >> CAS DataBase List >>2-Fluorophenylboronic acid

2-Fluorophenylboronic acid

CAS No.
1993-03-9
Chemical Name:
2-Fluorophenylboronic acid
Synonyms
2-Fluorophenylboronic;2-Flurorphenylboronic acid;2-FLUOROBENZENEBORONIC ACID;AKOS BRN-0104;2-fluoroborate;RARECHEM AH PB 0215;2-Fluorophenylboroni;o-Fluorphenylborsaeure;Tavaborole Impurity 30;uorobenzeneboronic acid
CBNumber:
CB4153982
Molecular Formula:
C6H6BFO2
Molecular Weight:
139.92
MDL Number:
MFCD00674013
MOL File:
1993-03-9.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 02:33:20
Product description Number Pack Size Price
2-Fluorophenylboronic acid ≥95% 445223 1g $73.2
2-Fluorophenylboronic acid ≥95% 445223 10g $657
2-Fluorophenylboronic Acid (contains varying amounts of Anhydride) F0407 1g $25
2-Fluorophenylboronic Acid (contains varying amounts of Anhydride) F0407 5g $72
2-Fluorophenylboronic acid Asreported 276070 5g $365
More product size

2-Fluorophenylboronic acid Properties

Melting point 101-110 °C (lit.)
Boiling point 267.8±42.0 °C(Predicted)
Density 1.24±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility soluble in Methanol
form Crystalline Powder
pka 8.32±0.58(Predicted)
color White to light yellow
BRN 3030413
InChI InChI=1S/C6H6BFO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4,9-10H
InChIKey QCSLIRFWJPOENV-UHFFFAOYSA-N
SMILES B(C1=CC=CC=C1F)(O)O
CAS DataBase Reference 1993-03-9(CAS DataBase Reference)
UNSPSC Code 12352103
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P280a-P304+P340-P305+P351+P338-P405-P501a
PPE Eyeshields, Gloves, type N95 (US)
Hazard Codes  Xn,Xi
Risk Statements  36/37/38-22
Safety Statements  37/39-26-36/37/39-27-24/25
WGK Germany  3
HazardClass  IRRITANT
HS Code  29319090
Storage Class 11 - Combustible Solids
NFPA 704
0
2 0

2-Fluorophenylboronic acid price More Price(101)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 445223 2-Fluorophenylboronic acid ≥95% 1993-03-9 1g $73.2 2026-04-30 Buy
Sigma-Aldrich 445223 2-Fluorophenylboronic acid ≥95% 1993-03-9 10g $657 2026-04-30 Buy
TCI Chemical F0407 2-Fluorophenylboronic Acid (contains varying amounts of Anhydride) 1993-03-9 1g $25 2026-04-30 Buy
TCI Chemical F0407 2-Fluorophenylboronic Acid (contains varying amounts of Anhydride) 1993-03-9 5g $72 2026-04-30 Buy
Usbiological 276070 2-Fluorophenylboronic acid Asreported 1993-03-9 5g $365 2026-06-03 Buy
Product number Packaging Price Buy
445223 1g $73.2 Buy
445223 10g $657 Buy
F0407 1g $25 Buy
F0407 5g $72 Buy
276070 5g $365 Buy

2-Fluorophenylboronic acid Chemical Properties,Uses,Production

Chemical Properties

white to light yellow crystalline powder

Uses

Used for the preparation of biologically active biphenyls and arylboron difluoride Lewis acids.

Uses

suzuki reaction

Uses

2-Fluorophenylboronic Acid, is used in Rh-catalyzed enantioselective addition reactions, and Rhodium and Palladium-catalyzed substitution reactions. It can also be used in the preparation of phenylboronic catechol esters as promising anion receptors for polymer electrolytes.

Synthesis

2-Bromofluorobenzene

1072-85-1

2-Fluorophenylboronic acid

1993-03-9

The general procedure for the synthesis of 2-fluorophenylboronic acid from o-bromofluorobenzene was as follows: 10.0 g (57.1 mmol) of 1-bromo-2-fluorobenzene and anhydrous tetrahydrofuran were added to a reaction flask and the mixture was subsequently cooled to -70 °C. At -70 °C, 44.2 ml (68.5 mmol) of 1.55 M n-butyllithium solution was slowly added dropwise to the reaction mixture. The temperature was maintained at -70 °C and stirring of the reaction mixture was continued for 1.5 hours. Subsequently, 21.5 g (114.2 mmol) of triisopropyl borate was added dropwise and the reaction temperature was gradually raised to room temperature and stirring was continued for 4 hours. Upon completion of the reaction, aqueous hydrochloric acid was added to the reaction mixture and extracted with dichloromethane. The organic phases were combined and the solvent was removed by distillation under reduced pressure to give the crude product of 2-fluorophenylboronic acid. The crude product was purified by column chromatography (eluent: hexane/acetone) to give 4.8 g (yield: 61%) of pure 2-fluorophenylboronic acid.

References

[1] Patent: US2012/273770, 2012, A1. Location in patent: Page/Page column 24
[2] Patent: US2004/6076, 2004, A1. Location in patent: Page 15
[3] Journal of Organic Chemistry, 2013, vol. 78, # 13, p. 6427 - 6439

1072-85-1
5419-55-6
1993-03-9
Synthesis of 2-Fluorophenylboronic acid from 2-Bromofluorobenzene and Triisopropyl borate
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View Lastest Price from 2-Fluorophenylboronic acid manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2-Fluorophenylboronic acid pictures 2025-09-25 2-Fluorophenylboronic acid
1993-03-9
$30.00 1KG 99% Henan Fengda Chemical Co., Ltd
2-Fluorophenylboronic acid pictures 2024-11-07 2-Fluorophenylboronic acid
1993-03-9
$5.00 1kg 99% 200000 Hebei Jingbo New Material Technology Co., Ltd
2-Fluorophenylboronic acid pictures 2022-10-09 2-Fluorophenylboronic acid
1993-03-9
$30.00-150.00 100Kg 99.0% up 50 tons per month Xinxiang Hongqi District Houyuan Trading Co.,Ltd
2-Fluorophenylboronic acid, May contain varying amounts of anhydride, 97% 2-Fluorophenylboroni 2-Fluorophenylboronic acid, 98% 1GR Boronic acid, B-(2-fluorophenyl)- BORONIC ACID, B-(2-FLUOROPHENYL)-; O-FLUORPHENYLBORSAEURE; o-Fluorphenylborsaeure o-fluoro-benzeneboronic acid 2-Fluorobenzeneboronic Acid (Contains Varying Amounts Of Anhydride) 2-Fluorobenzeneboronic acid 97% 2-Fluorobenzeneboronicacid97% 2-FLUOROPHENYLBORONIC ACID AKOS BRN-0104 O-FLUOROPHENYLBORONIC ACID RARECHEM AH PB 0215 ORTHOFLUOROPHENYLBORONIC ACID 2-Fluorophenylboronic Acid (contains varying amounts of Anhydride) 2-Fluorophenylboronic acid ,98% 2-fluoroborate uorobenzeneboronic acid 2-Fluorophenylboronic Acid extrapure, 97% 2-Fluorophenylboronic 2-FLUOROBENZENEBORONIC ACID 2-Flurorphenylboronic acid Vonoprazan Impurity 215 (2-Fluorophenyl)boronic acid - [F3340] Tavaborole Impurity 30 1993-03-9 199-33-9 1993-03-09 34-03-9 1993-09-3 93-03-9 3/9/1993 9/3/1993 1993-3-9 1993-03-4 1993/3/9 1933-03-9 C6H6BFO2 C6H6O2BF FC6H4BOH2 Aryl Boronic Acids and Derivatives Organometallic Reagents Boronic Acids B (Classes of Boron Compounds) Boronate Ester Potassium Trifluoroborate B (Classes of Boron Compounds) Boronic Acids Boronic Acids Boronic Acids and Derivatives Substituted Boronic Acids blocks BoronicAcids FluoroCompounds Boronic Acid Aryl
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