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Molecule
ID:10779
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₈BFO₃
Molecular Mass
169.9460232
Exact Mass
170.05505274
Charge
0
InChI
InChI=1S/C7H8BFO3/c1-12-7-3-2-5(8(10)11)4-6(7)9/h2-4,10-11H,1H3
InChIKey
IILGLPAJXQMKGQ-UHFFFAOYSA-N
Canonic Smiles
COc1ccc(cc1F)B(O)O
Isomeric Smiles
c1c(c(cc(c1)B(O)O)F)OC
Calculated Properties
JChem
Acid pKa
8.7248745
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
1.5263427
LogD (pH = 7.4)
1.506624
Log P
1.5266
Molar Refractivity
37.2831
Polarizability
15.783017
Polar Surface Area
49.69
Rotatable Bonds
2
Lipinski's Rule of Five
true
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
No Data Available
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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General Information
Calculated Properties
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RDKit
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IUPAC Traditional name
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IUPAC name
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Synonyms
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Physical Property
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Product Information
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
ChemBridge
4003303
Matrix Scientific
007687
Apollo Scientific
PC2902
Sigma Aldrich
564036
Chemik
CBC03000
Alfa Aesar
L19818
Bide Pharmatech
BD8171
A&J Pharmtech
AJA-O40161
Academic Data
PubChem
2782194
Names and Identifiers
IUPAC Traditional name
3-fluoro-4-methoxyphenylboronic acid
IUPAC name
(3-fluoro-4-methoxyphenyl)boronic acid
Synonyms
3-Fluoro-4-methoxyphenylboronic acid
(3-fluoro-4-methoxyphenyl)boronic acid
3-Fluoro-4-methoxyphenylboronic acid
3-Fluoro-4-methoxybenzeneboronic acid
3-Fluoro-4-methyloxyphenylboronic acid
3-氟-4-甲氧基苯硼酸
4-Methoxy-3-fluorophenylboronic acid
3-Fluoro-4-methoxyphenylboronic acid
3-Fluoro-4-methoxybenzeneboronic acid
3-Fluoro-4-methoxybenzeneboronic acid
Registration numbers
CAS Number
149507-26-6
MDL Number
MFCD00807404
PubChem SID
24880146
160974086
PubChem CID
2782194
Beilstein Number
7370120
EC Number
000-000-0
Molecule Details
Sigma Aldrich
564036
General description
Contains varying amounts of anhydride
Packaging
1, 5 g in glass bottle
Application
Reactant for:
• Preparation of hydroxyphenylnaphthols as 17β-hydroxysteroid dehydrogenase Type 2 inhibitors1
• Regioselective Suzuki coupling2
• Ruthenium-catalyzed arylation reactions3
• Synthesis of amino-trimethoxyphenyl-aryl thiazoles as microtubule inhibitors and potential antitumors4
• Rhodium catalyzed cyanation5
• Petasis reaction6
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
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CAS Number
•
MDL Number
•
PubChem SID
•
PubChem CID
•
Beilstein Number
•
EC Number
Properties
Safety Information
TSCA Listed
false
Source
否
Source
MSDS Link
Download link
Source
Download link
Source
Storage Warning
IRRITANT
Source
Irritant
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
3
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Irritant (Xi)
36/37/38
Source
H315
-
H319
-
H335
Source
26
-
37
Source
Physical Property
237-239°C
Source
206-211 °C(lit.)
Source
237-239°C
Source
Product Information
FC6H3(OCH3)B(OH)2
Source
98%
Source
98+%
Source
Source
Source
Personal Protective Equipment
German water hazard class
GHS Precautionary statements
GHS Pictograms
European Hazard Symbols
Risk Statements
GHS Hazard statements
Safety Statements
Melting Point
Linear Formula
Purity