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Molecule
ID:10554
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/c1-12-6-4-2-3-5(7(6)9)8(10)11/h2-4,10-11H,1H3
InChIKey
JCKZNMSBFBPDPM-UHFFFAOYSA-N
Canonic Smiles
COc1cccc(c1F)B(O)O
Isomeric Smiles
c1cc(c(c(c1)B(O)O)F)OC
Calculated Properties
JChem
Acid pKa
8.114373
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
1.5255517
LogD (pH = 7.4)
1.4503028
Log P
1.5266
Molar Refractivity
37.2831
Polarizability
15.785165
Polar Surface Area
49.69
Rotatable Bonds
2
Lipinski's Rule of Five
true
Data Source
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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
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IUPAC Traditional name
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IUPAC name
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Related Proteins
Molecular Spectra
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Sigma Aldrich
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
007381
Apollo Scientific
PC10096
Sigma Aldrich
594253
Chemik
CBC02700
Alfa Aesar
L19655
Bide Pharmatech
BD4904
A&J Pharmtech
AJA-O35625
Academic Data
PubChem
4985744
Names and Identifiers
Synonyms
2-Fluoro-3-methoxyphenylboronic acid
2-Fluoro-3-methoxybenzeneboronic acid
2-Fluoro-3-methoxyphenylboronic acid
2-氟-3-甲氧基苯硼酸
2-Fluoro-3-methoxybenzeneboronic acid
2-Fluoro-3-methoxyphenylboronic acid
IUPAC Traditional name
2-fluoro-3-methoxyphenylboronic acid
IUPAC name
(2-fluoro-3-methoxyphenyl)boronic acid
Registration numbers
EC Number
000-000-0
MDL Number
MFCD02094728
CAS Number
352303-67-4
Beilstein Number
9191510
PubChem SID
160973861
24881492
PubChem CID
4985744
Properties
Product Information
Purity
97%
Source
98%
Source
Linear Formula
FC6H3(OCH3)B(OH)2
Source
Safety Information
MSDS Link
Download link
Source
Download link
Source
Storage Warning
IRRITANT
Source
Irritant/Store under Argon/Keep Cold
Source
TSCA Listed
false
Source
否
Source
German water hazard class
3
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
Safety Statements
26
-
37
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
European Hazard Symbols
Irritant (Xi)
Source
Risk Statements
36/37/38
Source
GHS Precautionary statements
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
GHS Pictograms
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
Source
Physical Property
Melting Point
117-122°C
Source
117-122 °C(lit.)
Source
Molecule Details
Sigma Aldrich
594253
Other Notes
Contains varying amounts of anhydride
Packaging
1, 5 g in glass bottle
Application
Reactant for:
• Regioselective Suzuki coupling1
• Preparation of inhibitors of 17β-hydroxysteroid dehydrogenase type 12
• Preparation of boronic esters3
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
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EC Number
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PubChem CID