2-Fluorophenylboronic acid - ≥98% , CAS No.1993-03-9

CAS: 1993-03-9 Cat. No.: F103267 Formula: C6H6BFO2 Molecular Weight: 139.92 EC Number: 671-858-7
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
o-fluorobenzeneboronic acid | O-FLUORO-BENZENEBORONIC ACID | FT-0612449 | EN300-88718 | MFCD00674013 | (2-Fluorophenyl)boronato(2-) | DTXSID30941836 | (2-fluorophenyl) boronic acid | (2-fluorophenyl)boranediol | 2-fluorobenzene boronic acid | (2-fluorophe
Storage
Store at 2-8°C
Shipped In
Wet ice
Size
USA
Germany (EU)*
Price
Qty
1g
F103267-1g
1 In stock
$9.90
5g
F103267-5g
1 In stock
$10.90
25g
F103267-25g
2 In stock

$24.90

$37.90
Save $13.00 (34.30%)
100g
F103267-100g
Made to order · 8–12 wks

$87.90

$131.90
Save $44.00 (33.36%)
500g
F103267-500g
Made to order · 8–12 wks

$423.90

$635.90
Save $212.00 (33.34%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Reactant for: · Preparation of phenylboronic catechol esters as promising anion receptors for polymer electrolytes · Diastereoselective synthesis of trisubstituted allylic alcohols via rhodium-catalyzed arylation · Site-selective Suzuki-Miyaura arylation reactions · Rh-catalyzed enantioselective addition reactions · Rhodium- and Palladium-catalyzed substitution reactions

Specifications

Synonyms
o-fluorobenzeneboronic acid | O-FLUORO-BENZENEBORONIC ACID | FT-0612449 | EN300-88718 | MFCD00674013 | (2-Fluorophenyl)boronato(2-) | DTXSID30941836 | (2-fluorophenyl) boronic acid | (2-fluorophenyl)boranediol | 2-fluorobenzene boronic acid | (2-fluorophe
Specifications & Purity
≥98%
Storage
Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥98%
Names and Identifiers
Pubchem Sid528756468
Canonical SmilesB(C1=CC=CC=C1F)(O)O
IUPAC Name(2-fluorophenyl)boronic acid
InChIKeyQCSLIRFWJPOENV-UHFFFAOYSA-N
INCHI1S/C6H6BFO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4,9-10H
Isomeric SMILES B(C1=CC=CC=C1F)(O)O
WGK Germany 3
Molecular Weight 139.92
Reaxy-Rn 3030413
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3030413&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClassBenzene and substituted derivatives
SubclassHalobenzenes
Intermediate Tree Nodes Not available
Direct ParentFluorobenzenes
Alternative Parents Aryl fluorides  Boronic acids  Organic metalloid salts  Organofluorides  Organoboron compounds  Organic oxygen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Fluorobenzene - Aryl halide - Aryl fluoride - Boronic acid - Boronic acid derivative - Organic metalloid salt - Organic oxygen compound - Hydrocarbon derivative - Organic salt - Organofluoride - Organoboron compound - Organohalogen compound - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as fluorobenzenes. These are compounds containing one or more fluorine atoms attached to a benzene ring.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
MGLL Tchem Monoglyceride lipase (1909 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Faah Anandamide amidohydrolase (3907 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

7 results found

Lot NumberCertificate TypeDateItem
L2423573Certificate of AnalysisJul 12, 2024 F103267
L2423574Certificate of AnalysisJul 12, 2024 F103267
K1926164Certificate of AnalysisSep 08, 2023 F103267
L1418021Certificate of AnalysisSep 13, 2022 F103267
A2404255Certificate of AnalysisJul 27, 2021 F103267
H2513161Certificate of AnalysisJul 27, 2021 F103267
L2403097Certificate of AnalysisJul 27, 2021 F103267
Chemical and Physical Properties
SolubilitySoluble in Methanol
Melt Point(°C)101-110°C
Molecular Weight139.920 g/mol
XLogP3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass140.044 Da
Monoisotopic Mass140.044 Da
Topological Polar Surface Area40.500 Ų
Heavy Atom Count10
Formal Charge0
Complexity110.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Solution Calculators
Reviews

Customer Reviews

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