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Molecule
ID:41755
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₈N₂O₂
Molecular Mass
188.18272
Exact Mass
188.05857751
Charge
0
InChI
InChI=1S/C10H8N2O2/c13-10(14)8-3-4-9(11-7-8)12-5-1-2-6-12/h1-7H,(H,13,14)
InChIKey
GXLGOBAHBJQAJB-UHFFFAOYSA-N
Canonic Smiles
OC(=O)c1ccc(nc1)n1cccc1
Isomeric Smiles
n1(c2ncc(C(=O)O)cc2)cccc1
Calculated Properties
JChem
Acid pKa
1.9279152
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
-0.26014477
LogD (pH = 7.4)
-1.8566208
Log P
0.58487767
Molar Refractivity
61.2232
Polarizability
19.082508
Polar Surface Area
55.12
Rotatable Bonds
2
Lipinski's Rule of Five
true
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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
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Data Source
Commercial Catalog
Matrix Scientific
044937
Apollo Scientific
OR14393
Key Organics
5Y-0705
Enamine
EN300-102964
Academic Data
PubChem
2764100
Names and Identifiers
IUPAC Traditional name
6-(pyrrol-1-yl)pyridine-3-carboxylic acid
Synonyms
6-(1H-Pyrrol-1-yl)pyridine-3-carboxylic acid
6-(1H-Pyrrol-1-yl)nicotinic acid
1-(3-Carboxypyridin-6-yl)-1H-pyrrole
6-(1H-pyrrol-1-yl)pyridine-3-carboxylic acid
IUPAC name
6-(1H-pyrrol-1-yl)pyridine-3-carboxylic acid
Registration numbers
CAS Number
175135-86-1
MDL Number
MFCD00067843
PubChem SID
162046518
PubChem CID
2764100
Properties
Safety Information
Storage Warning
IRRITANT
Source
Irritant
Source
TSCA Listed
false
Source
MSDS Link
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Product Information
Purity
>95%
Source
> 95%
Source
95%
Source
Physical Property
Melting Point
289-291°C
Source
289 - 291 °C
Source
259 - 261°C
Source
Hydrophobicity(logP)
2.188
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay