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Molecule
ID:70137
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₉NO₂
Molecular Mass
151.16256
Exact Mass
151.06332853
Charge
0
InChI
InChI=1S/C8H9NO2/c1-2-11-8(10)7-5-3-4-6-9-7/h3-6H,2H2,1H3
InChIKey
FQYYIPZPELSLDK-UHFFFAOYSA-N
Canonic Smiles
CCOC(=O)c1ccccn1
Isomeric Smiles
c1(ccccn1)C(=O)OCC
Calculated Properties
JChem
H Acceptors
2
H Donor
0
LogD (pH = 5.5)
1.3015071
LogD (pH = 7.4)
1.3017061
Log P
1.3017086
Molar Refractivity
40.303
Polarizability
15.706331
Polar Surface Area
39.19
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
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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
Data Source
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Commercial Catalog
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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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Safety Information
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Product Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
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MP Biomedicals
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Sigma Aldrich
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TRC
References
•
PubChem Literature
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From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR4533
MP Biomedicals
02156251
Sigma Aldrich
E45414
80300
TRC
P437235
Chemik
CHH00309
Matrix Scientific
075663
Bide Pharmatech
BD19696
Alfa Aesar
A13973
Academic Data
PubChem
17307
Names and Identifiers
Synonyms
Ethyl pyridine-2-carboxylate
Ethyl 2-picolinate
Ethyl 2-picolinate
PICOLINIC ACID ETHYL ESTER
Ethyl Picolinate
Ethyl pyridine-2-carboxylate
吡啶-2-甲酸乙酯
2-吡啶甲酸乙酯
2-(Ethoxycarbonyl)pyridine
Ethyl 2-picolinate
2-Pyridinecarboxylic Acid Ethyl Ester
Ethyl 2-Pyridinecarboxylate
Ethyl picolinate
Picolinic acid ethyl ester
吡啶-2-甲酸乙酯
IUPAC Traditional name
picolinic acid, ethyl ester
IUPAC name
ethyl pyridine-2-carboxylate
Registration numbers
MDL Number
MFCD00006292
CAS Number
2524-52-9
EC Number
219-758-0
Beilstein Number
122485
PubChem SID
24894562
162035862
PubChem CID
17307
Molecule Details
MP Biomedicals
02156251
1 ml = approx. 1.12 g
Sigma Aldrich
E45414
Packaging
25 g in glass bottle
TRC
P437235
Used in the preparation of 2-Aminodihydro[1,3]thiazines as BACE 2 inhibitors and their preparation and use in the treatment of diabetes.
References
PubChem Literature
From Data Sources
•
Ciayadi, R., et al.: Bioorg. Med. Chem. Lett., 21, 5642 (2011)
Bioactivity
PubChem BioAssay
Registration numbers
•
MDL Number
•
CAS Number
•
EC Number
•
Beilstein Number
•
PubChem SID
•
PubChem CID
Properties
Safety Information
MSDS Link
Download link
Source
Download link
Source
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Source
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Source
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Source
Storage Warning
IRRITANT
Source
Irritant
Source
TSCA Listed
false
Source
是
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
H319
Source
German water hazard class
3
Source
GHS Signal Word
Warning
Source
Risk Statements
36/37/38
Source
36
Source
European Hazard Symbols
Irritant (Xi)
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
Personal Protective Equipment
Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
Source
Safety Statements
26
-
36
Source
26
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P305+P351+P338
Source
Product Information
Purity
95+%
Source
99%
Source
≥99.0% (GC)
Source
98%
Source
Certificate of Analysis
Download link
Source
Download link
Source
C8H9NO2
Source
purum
Source
Physical Property
Density
1.12 g/ml
Source
1.119 g/mL at 25 °C(lit.)
Source
1.120
Source
Refractive Index
n20/D 1.511(lit.)
Source
n20/D 1.511
Source
1.5105
Source
Flash Point
107 °C
Source
224.6 °F
Source
107°C(224°F)
Source
240-241 °C(lit.)
Source
239-241°C
Source
2 °C(lit.)
Source
1-3°C
Source
Empirical Formula (Hill Notation)
Grade
Boiling Point
Melting Point