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Molecule
ID:8420
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₁₁BO₄
Molecular Mass
181.98154
Exact Mass
182.07503923
Charge
0
InChI
InChI=1S/C8H11BO4/c1-12-6-4-3-5-7(13-2)8(6)9(10)11/h3-5,10-11H,1-2H3
InChIKey
BKWVXPCYDRURMK-UHFFFAOYSA-N
Canonic Smiles
COc1cccc(c1B(O)O)OC
Isomeric Smiles
c1(c(cccc1OC)OC)B(O)O
Calculated Properties
JChem
Acid pKa
8.114278
H Acceptors
4
H Donor
2
LogD (pH = 5.5)
1.1333514
LogD (pH = 7.4)
1.0580804
Log P
1.1344
Molar Refractivity
43.5299
Polarizability
18.590307
Polar Surface Area
58.92
Rotatable Bonds
3
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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JChem
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Academic Data
Names and Identifiers
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IUPAC Traditional name
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Synonyms
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IUPAC name
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Properties
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Product Information
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Safety Information
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Physical Property
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
•
PubChem BioAssay
Data Source
Commercial Catalog
ChemBridge
3200972
Matrix Scientific
004014
Apollo Scientific
OR4443
Sigma Aldrich
480096
Enamine
EN300-119838
Bide Pharmatech
BD5278
Alfa Aesar
B24305
A&J Pharmtech
AJA-O40564
Academic Data
PubChem
2734343
Names and Identifiers
IUPAC Traditional name
2,6-dimethoxyphenylboronic acid
Synonyms
(2,6-dimethoxyphenyl)boronic acid
2,6-Dimethoxyphenylboronic acid
2,6-二甲氧基苯硼酸
2,6-Dimethoxyphenylboronic acid
2,6-Dimethoxybenzeneboronic acid
2,6-Dimethoxybenzeneboronic acid
2,6-Dimethoxyphenylboronic acid
2,6-Dimethoxybenzeneboronic acid
IUPAC name
(2,6-dimethoxyphenyl)boronic acid
Registration numbers
CAS Number
23112-96-1
MDL Number
MFCD01318987
PubChem CID
2734343
PubChem SID
160971727
24871546
Beilstein Number
3032352
Properties
Product Information
Purity
97%
Source
95%
Source
97+%
Source
98%
Source
Linear Formula
(CH3O)2C6H3B(OH)2
Source
Safety Information
Storage Warning
IRRITANT
Source
Irritant/Keep Cold
Source
TSCA Listed
false
Source
否
Source
MSDS Link
Download link
Source
Download link
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
German water hazard class
3
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
Risk Statements
36/37/38
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
European Hazard Symbols
Irritant (Xi)
Source
Safety Statements
26
-
37
Source
GHS Precautionary statements
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
Physical Property
Melting Point
110-112°C
Source
110-112 °C(lit.)
Source
111 - 112°C
Source
106-108°C
Source
Hydrophobicity(logP)
1.603
Source
Molecule Details
Sigma Aldrich
480096
Other Notes
Contains varying amounts of anhydride
Packaging
5, 25 g in glass bottle
Application
Reactant for:
• Suzuki-Miyaura reactions1,2,3,4,5
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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MDL Number
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PubChem CID
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PubChem SID
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Beilstein Number