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Molecule
ID:15463
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₆N₂O₂
Molecular Mass
138.12404
Exact Mass
138.04292744
Charge
0
InChI
InChI=1S/C6H6N2O2/c7-5-4(6(9)10)2-1-3-8-5/h1-3H,(H2,7,8)(H,9,10)
InChIKey
KPIVDNYJNOPGBE-UHFFFAOYSA-N
Canonic Smiles
OC(=O)c1cccnc1N
Isomeric Smiles
c1cnc(c(c1)C(=O)O)N
Calculated Properties
JChem
LogD (pH = 7.4)
-1.47
LogD (pH = 5.5)
-0.90
Log P
-0.89
Rotatable Bonds
1
H Donor
2
H Acceptors
4
Lipinski's Rule of Five
true
Acid pKa
1.37
Polar Surface Area
76.21
Polarizability
12.66
Molar Refractivity
36.17
LOG S
-0.69
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
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ChEBI
References
•
PubChem Literature
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From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR18366
MP Biomedicals
05209790
Matrix Scientific
016028
InterBioScreen
BB_SC-3260
Sigma Aldrich
A68300
08810
TRC
A618380
Bide Pharmatech
BD7976
Alfa Aesar
A11195
A&J Pharmtech
AJA-O38353
Academic Data
PubChem
72930
ChEBI
CHEBI:68572
Names and Identifiers
Synonyms
2-Aminopyridine-3-carboxylic acid
2-Amino-3-carboxypyridine
2-Aminonicotinic acid 98%
2-Aminopyridine-3-carboxylic acid
2-AMINONICOTINIC ACID
2-氨基烟酸
2-Aminonicotinic acid
2-Amino-3-pyridinecarboxylic Acid
2-氨基吡啶-3-羧酸
NSC 3049
2-Amino Nicotinic Acid
2-氨基烟酸
2-氨基吡啶-3-羧酸
2-Aminonicotinic acid
2-Aminopyridine-3-carboxylic acid
2-aminonicotinic acid
IUPAC Traditional name
2-aminopyridine-3-carboxylic acid
2-aminonicotinic acid
IUPAC name
2-aminopyridine-3-carboxylic acid
Registration numbers
CAS Number
5345-47-1
MDL Number
MFCD00006318
EC Number
226-296-3
Beilstein Number
119031
PubChem CID
72930
PubChem SID
24891144
160978770
24846223
160645701
CompTox Database
DTXSID1063801
PubMed Citation Links
22770225
MetaboLights Database
MTBLS1693
MTBLS1903
BRENDA Ligand Database
220471
BRENDA Database
1.4.3.1
BindingDB Database
50122000
CHEBI ID
CHEBI:68572
Reaxys Registry
119031
CHEMBL
CHEMBL3322868
BKMS React Database
220471
SureChEMBL Database
SCHEMBL181403
ACToR Database
5345-47-1
NMRShiftDB Database
20040335
Molecule Details
MP Biomedicals
05209790
MP Biomedicals Rare Chemical collection
Sigma Aldrich
A68300
Packaging
5, 25 g in glass bottle
TRC
A618380
A component of hair dyes.
ChEBI
CHEBI:68572
An aminonicotinic acid in which the amino group is situated at position 2 of the pyridine ring.
References
PubChem Literature
From Data Sources
•
Barrett, O.J., et al.: ChemBioChem., 7, 1882 (2006)
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
MDL Number
•
EC Number
•
Beilstein Number
•
PubChem CID
•
PubChem SID
•
CompTox Database
•
PubMed Citation Links
•
MetaboLights Database
•
BRENDA Ligand Database
•
BRENDA Database
•
BindingDB Database
•
CHEBI ID
•
Reaxys Registry
•
CHEMBL
•
BKMS React Database
•
SureChEMBL Database
•
ACToR Database
•
NMRShiftDB Database
Properties
Safety Information
MSDS Link
Download link
Source
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Source
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Source
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Source
true
Source
是
Source
IRRITANT
Source
Irritant
Source
3
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
Refrigerator
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
Irritant (Xi)
26
-
37
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
36/37/38
Source
H315
-
H319
-
H335
Source
Product Information
98%
Source
≥97.0% (T)
Source
98+%
Source
Download link
Source
Download link
Source
C6H6N2O2
Source
Physical Property
296-298°C
Source
300°C
Source
295-297 °C (dec.)(lit.)
Source
>265°C (dec.)
Source
ca 298°C dec.
Source
White to Off-White
Source
DMSO
Source
Source
purum
Source
Source
TSCA Listed
Storage Warning
German water hazard class
Personal Protective Equipment
Storage Condition
GHS Precautionary statements
European Hazard Symbols
Safety Statements
GHS Pictograms
Risk Statements
GHS Hazard statements
Purity
Certificate of Analysis
Empirical Formula (Hill Notation)
Melting Point
Apperance
Solubility
Grade