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Molecule
ID:32708
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₁₁BO₂
Molecular Mass
149.98274
Exact Mass
150.08520999
Charge
0
InChI
InChI=1S/C8H11BO2/c1-2-7-5-3-4-6-8(7)9(10)11/h3-6,10-11H,2H2,1H3
InChIKey
QSSPYZOSTJDTTL-UHFFFAOYSA-N
Canonic Smiles
CCc1ccccc1B(O)O
Isomeric Smiles
c1(c(cccc1)CC)B(O)O
Calculated Properties
JChem
Acid pKa
8.808417
H Acceptors
2
H Donor
2
LogD (pH = 5.5)
2.5030878
LogD (pH = 7.4)
2.486754
Log P
2.5033
Molar Refractivity
40.2457
Polarizability
17.142221
Polar Surface Area
40.46
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
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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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Physical Property
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Related Proteins
Molecular Spectra
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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
Matrix Scientific
035422
Apollo Scientific
OR11254
Sigma Aldrich
521523
Alfa Aesar
L17719
Chemik
CBC00115
Bide Pharmatech
BD5261
A&J Pharmtech
AJA-O35589
Academic Data
PubChem
4100862
Names and Identifiers
IUPAC Traditional name
2-ethylphenylboronic acid
Synonyms
2-Ethylphenylboronic acid
2-Ethylbenzeneboronic acid
2-乙基苯硼酸
2-Ethylphenylboronic acid
o-Ethylphenylboronic acid
2-Ethylbenzeneboronic acid
2-Ethylphenylboronic acid
2-Ethylbenzeneboronic acid
IUPAC name
(2-ethylphenyl)boronic acid
Registration numbers
CAS Number
90002-36-1
PubChem CID
4100862
PubChem SID
160996015
24874212
MDL Number
MFCD02093075
Beilstein Number
2963801
EC Number
000-000-0
Molecule Details
Sigma Aldrich
521523
Other Notes
Contains varying amounts of anhydride
Packaging
10 g in glass bottle
Application
Reactant for:
• Palladium-catalyzed cross-coupling1
• Enantioselective Hayashi-Miyaura reaction2
• Pd-catalyzed Suzuki-Miyaura reaction3,4
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
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CAS Number
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PubChem CID
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PubChem SID
•
MDL Number
•
Beilstein Number
•
EC Number
Properties
Safety Information
MSDS Link
Download link
Source
Download link
Source
TSCA Listed
false
Source
否
Source
Storage Warning
IRRITANT
Source
Irritant
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
3
Source
26
-
37
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
H315
-
H319
-
H335
Source
36/37/38
Source
Irritant (Xi)
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
Physical Property
102.5-107.5 °C(lit.)
Source
96-98°C
Source
Product Information
C2H5C6H4B(OH)2
Source
98%
Source
98+%
Source
Source
Source
Personal Protective Equipment
German water hazard class
Safety Statements
GHS Pictograms
GHS Hazard statements
Risk Statements
European Hazard Symbols
GHS Precautionary statements
Melting Point
Linear Formula
Purity