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Molecule
ID:32625
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₃H₁₃BO₃
Molecular Mass
228.05152
Exact Mass
228.09577468
Charge
0
InChI
InChI=1S/C13H13BO3/c15-14(16)12-8-4-5-9-13(12)17-10-11-6-2-1-3-7-11/h1-9,15-16H,10H2
InChIKey
MCAIDINWZOCYQK-UHFFFAOYSA-N
Canonic Smiles
OB(c1ccccc1OCc1ccccc1)O
Isomeric Smiles
c1(c(cccc1)OCc1ccccc1)B(O)O
Calculated Properties
JChem
Acid pKa
8.4153
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
3.1631753
LogD (pH = 7.4)
3.1238806
Log P
3.1637
Molar Refractivity
61.6793
Polarizability
25.647709
Polar Surface Area
49.69
Rotatable Bonds
4
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
No Data Available
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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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JChem
Data Source
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Academic Data
Names and Identifiers
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Synonyms
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IUPAC Traditional name
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IUPAC name
Registration numbers
Properties
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Physical Property
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Product Information
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
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TRC
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
035335
Apollo Scientific
OR10360
Sigma Aldrich
521337
TRC
B287740
Alfa Aesar
L20100
Bide Pharmatech
BD14645
A&J Pharmtech
AJA-O35201
Academic Data
PubChem
2773253
Names and Identifiers
Synonyms
2-(Benzyloxy)benzeneboronic acid
2-Benzyloxyphenylboronic acid
2-苯甲氧基苯硼酸
2-Benzyloxybenzeneboronic acid
2-Benzyloxyphenylboronic acid
2-Benzyloxyphenylborornic acid
2-(Phenylmethoxy)benzeneboronic acid
[2-[(Phenylmethyl)oxy]phenyl]boronic Acid
2-苄氧基苯硼酸
2-(Phenylmethyl)oxyphenylboronic acid
B-[2-(Phenylmethoxy)phenyl]boronic Acid
2-(Benzyloxy)phenylboronic acid
IUPAC Traditional name
2-(benzyloxy)phenylboronic acid
IUPAC name
[2-(benzyloxy)phenyl]boronic acid
Registration numbers
CAS Number
190661-29-1
MDL Number
MFCD01632206
PubChem SID
160995932
24874201
PubChem CID
2773253
Beilstein Number
7813704
Molecule Details
Sigma Aldrich
521337
Other Notes
Contains varying amounts of anhydride
Packaging
1, 5 g in glass bottle
Application
Reactant for:
• Palladium complex-catalyzed selective hydroxylation1
• Palladium(II)-catalyzed oxidative Heck reactions2
• Metal-free electrophilic fluorination3
• Suzuki-Miyaura cross-coupling reactions4
TRC
B287740
Reagent used in the preparation of different kinase inhibitors.
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
MDL Number
•
PubChem SID
•
PubChem CID
•
Beilstein Number
Properties
Safety Information
MSDS Link
Download link
Source
Download link
Source
Download link
Source
TSCA Listed
false
Source
否
Source
IRRITANT, CORROSIVE
Source
Harmful/Irritant/Keep Cold/Store under Argon
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
3
Source
-20°C Freezer
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
P261
-P280G-
P305+P351+P338
Source
26
-
37
Source
Irritant (Xi)
H315
-
H319
-
H335
Source
36/37/38
Source
Physical Property
105-110°C
Source
105-110 °C(lit.)
Source
96-99°C
Source
Ethyl Acetate
Source
Dichloromethane
Source
Methanol
Source
White Solid
Source
Product Information
C6H5CH2OC6H4B(OH)2
Source
Download link
Source
96%
Source
98%
Source
Source
Source
Storage Warning
Personal Protective Equipment
German water hazard class
Storage Condition
GHS Pictograms
GHS Precautionary statements
Safety Statements
European Hazard Symbols
GHS Hazard statements
Risk Statements
Melting Point
Solubility
Apperance
Linear Formula
Certificate of Analysis
Purity