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Molecule
ID:10044
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₈BNO₃
Molecular Mass
152.94362
Exact Mass
153.05972352
Charge
0
InChI
InChI=1S/C6H8BNO3/c1-11-6-3-2-5(4-8-6)7(9)10/h2-4,9-10H,1H3
InChIKey
DHADXDMPEUWEAS-UHFFFAOYSA-N
Canonic Smiles
COc1ccc(cn1)B(O)O
Isomeric Smiles
c1(cnc(cc1)OC)B(O)O
Calculated Properties
JChem
Acid pKa
8.5298
H Acceptors
4
H Donor
2
LogD (pH = 5.5)
0.77332336
LogD (pH = 7.4)
0.7428904
Log P
0.7738
Molar Refractivity
35.2233
Polarizability
15.184434
Polar Surface Area
62.58
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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IUPAC name
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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
Apollo Scientific
OR7235
Matrix Scientific
006786
Sigma Aldrich
637610
Alfa Aesar
L20087
Enamine
EN300-56543
Bide Pharmatech
BD3675
A&J Pharmtech
AJA-O35570
Academic Data
PubChem
2734368
Names and Identifiers
Synonyms
2-Methoxy-5-pyridineboronic acid
2-Methoxypyridine-5-boronic acid
2-甲氧基吡啶-5-硼酸
2-Methoxy-5-pyridylboronic acid
2-Methoxypyridine-5-boronic acid
2-甲氧基-5-吡啶硼酸
6-甲氧基-3-吡啶硼酸
6-Methoxy-3-pyridinylboronic acid
2-Methoxy-5-pyridineboronic acid
(6-methoxypyridin-3-yl)boranediol
IUPAC name
(6-methoxypyridin-3-yl)boronic acid
IUPAC Traditional name
6-methoxypyridin-3-ylboronic acid
Registration numbers
PubChem CID
2734368
PubChem SID
160973351
24882872
MDL Number
MFCD02093044
CAS Number
163105-89-3
Beilstein Number
9119950
Molecule Details
Sigma Aldrich
637610
Other Notes
Contains varying amounts of anhydride
Packaging
1, 5 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
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PubChem CID
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PubChem SID
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MDL Number
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CAS Number
•
Beilstein Number
Properties
Safety Information
TSCA Listed
false
Source
否
Source
Storage Warning
IRRITANT, AIR SENSITIVE, KEEP COLD
Source
Irritant
Source
MSDS Link
Download link
Source
Download link
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
2-8°C
Source
3
Source
Irritant (Xi)
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
26
-
37
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
Product Information
95%
Source
≥95.0%
Source
95+%
Source
98%
Source
C6H8BNO3
Source
Physical Property
135-140 °C(lit.)
Source
132-133°C
Source
0.918
Source
Source
Source
Personal Protective Equipment
Storage Temperature
German water hazard class
European Hazard Symbols
GHS Pictograms
GHS Hazard statements
Risk Statements
Safety Statements
GHS Precautionary statements
Purity
Empirical Formula (Hill Notation)
Melting Point
Hydrophobicity(logP)