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Molecule
ID:42202
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₄BrNO₃
Molecular Mass
218.00486
Exact Mass
216.93745499
Charge
0
InChI
InChI=1S/C6H4BrNO3/c7-4-1-3(6(10)11)2-8-5(4)9/h1-2H,(H,8,9)(H,10,11)
InChIKey
PQDLYKZCJBGXPQ-UHFFFAOYSA-N
Canonic Smiles
OC(=O)c1c[nH]c(=O)c(c1)Br
Isomeric Smiles
c1(cc(c(=O)[nH]c1)Br)C(=O)O
Calculated Properties
JChem
Acid pKa
2.3536222
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
-2.7188656
LogD (pH = 7.4)
-3.239931
Log P
0.27740937
Molar Refractivity
41.6538
Polarizability
15.424026
Polar Surface Area
66.4
Rotatable Bonds
1
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
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IUPAC Traditional name
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IUPAC name
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CAS Number
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PubChem SID
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PubChem CID
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Physical Property
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Product Information
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Molecular Spectra
Molecule Details
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
045437
Key Organics
7W-0338
Enamine
EN300-90349
Academic Data
PubChem
2764314
Names and Identifiers
Synonyms
5-Bromo-6-oxo-1,6-dihydro-3-pyridinecarboxylic acid
5-bromo-6-oxo-1,6-dihydropyridine-3-carboxylic acid
IUPAC Traditional name
5-bromo-6-oxo-1H-pyridine-3-carboxylic acid
IUPAC name
5-bromo-6-oxo-1,6-dihydropyridine-3-carboxylic acid
Registration numbers
MDL Number
MFCD03791237
CAS Number
41668-13-7
PubChem SID
162046965
PubChem CID
2764314
Properties
Safety Information
Storage Warning
IRRITANT
Source
TSCA Listed
false
Source
MSDS Link
Download link
Source
Physical Property
Melting Point
334-336°C
Source
334 - 336 °C
Source
307 - 309°C
Source
Hydrophobicity(logP)
0.512
Source
Product Information
Purity
95+%
Source
>95%
Source
95%
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay