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Molecule
ID:22263
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₅H₄BrN₃O₂
Molecular Mass
218.00816
Exact Mass
216.94868838
Charge
0
InChI
InChI=1S/C5H4BrN3O2/c6-4-1-3(9(10)11)2-8-5(4)7/h1-2H,(H2,7,8)
InChIKey
OFXNHXMPRZDIDM-UHFFFAOYSA-N
Canonic Smiles
[O-][N+](=O)c1cnc(c(c1)Br)N
Isomeric Smiles
c1(cnc(c(c1)Br)N)[N+](=O)[O-]
Calculated Properties
JChem
Acid pKa
18.094288
H Acceptors
4
H Donor
1
LogD (pH = 5.5)
1.2298403
LogD (pH = 7.4)
1.2298417
Log P
1.2298418
Molar Refractivity
42.8583
Polarizability
15.613279
Polar Surface Area
82.05
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
No Data Available
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Molecular Spectra
No Data Available
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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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RDKit
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IUPAC Traditional name
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MDL Number
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PubChem CID
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PubChem SID
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Physical Property
Related Proteins
Molecular Spectra
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR5574
Matrix Scientific
024635
Enamine
EN300-93430
Bide Pharmatech
BD18635
A&J Pharmtech
AJA-O40233
Academic Data
PubChem
2734412
Names and Identifiers
IUPAC Traditional name
3-bromo-5-nitropyridin-2-amine
Synonyms
2-Amino-3-bromo-5-nitropyridine 98%
2-Amino-3-bromo-5-nitropyridine
3-bromo-5-nitropyridin-2-amine
IUPAC name
3-bromo-5-nitropyridin-2-amine
Registration numbers
CAS Number
15862-31-4
MDL Number
MFCD00955628
PubChem CID
2734412
PubChem SID
160985570
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Product Information
Purity
98%
Source
95%
Source
Safety Information
Storage Warning
IRRITANT
Source
Irritant
Source
TSCA Listed
false
Source
MSDS Link
Download link
Source
Physical Property
219-221°C
Source
1.281
Source
Melting Point
Hydrophobicity(logP)