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Molecule
ID:32706
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₁₀BNO₃
Molecular Mass
166.9702
Exact Mass
167.07537359
Charge
0
InChI
InChI=1S/C7H10BNO3/c1-2-12-7-6(8(10)11)4-3-5-9-7/h3-5,10-11H,2H2,1H3
InChIKey
FXUMKSCYKPOZOO-UHFFFAOYSA-N
Canonic Smiles
CCOc1ncccc1B(O)O
Isomeric Smiles
c1(c(cccn1)B(O)O)OCC
Calculated Properties
JChem
Acid pKa
8.06069
H Acceptors
4
H Donor
2
LogD (pH = 5.5)
1.1150082
LogD (pH = 7.4)
1.0308838
Log P
1.1163
Molar Refractivity
39.9719
Polarizability
17.018879
Polar Surface Area
62.58
Rotatable Bonds
3
Lipinski's Rule of Five
true
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Related Proteins
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Molecular Spectra
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Molecule Details
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Bioactivity
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Data Source
Commercial Catalog
Matrix Scientific
035420
Apollo Scientific
OR9499
Alfa Aesar
L20422
A&J Pharmtech
AJA-O30624
Academic Data
PubChem
11309733
Names and Identifiers
Synonyms
2-Ethoxypyridine-3-boronic acid
3-Borono-2-ethoxypyridine
2-Ethoxypyridine-3-boronic acid
2-乙氧基吡啶-3-硼酸
IUPAC name
(2-ethoxypyridin-3-yl)boronic acid
IUPAC Traditional name
2-ethoxypyridin-3-ylboronic acid
Registration numbers
CAS Number
854373-97-0
MDL Number
MFCD06201036
PubChem CID
11309733
PubChem SID
160996013
Properties
Safety Information
MSDS Link
Download link
Source
TSCA Listed
false
Source
否
Source
Storage Warning
IRRITANT
Source
Irritant/Store under Argon/Keep Cold
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
GHS Precautionary statements
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
Safety Statements
26
-
37
Source
European Hazard Symbols
Irritant (Xi)
Source
Risk Statements
36/37/38
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
Physical Property
Melting Point
102-104°C
Source
Product Information
Purity
98%
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay