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Molecule
ID:10547
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₃BrFNO₂
Molecular Mass
219.9959232
Exact Mass
218.93311856
Charge
0
InChI
InChI=1S/C6H3BrFNO2/c7-5-3-4(9(10)11)1-2-6(5)8/h1-3H
InChIKey
FAWMTDSAMOCUAR-UHFFFAOYSA-N
Canonic Smiles
[O-][N+](=O)c1ccc(c(c1)Br)F
Isomeric Smiles
c1cc(c(cc1[N+](=O)[O-])Br)F
Calculated Properties
JChem
H Acceptors
2
H Donor
0
LogD (pH = 5.5)
2.8246846
LogD (pH = 7.4)
2.8246846
Log P
2.8246846
Molar Refractivity
40.2177
Polarizability
15.111174
Polar Surface Area
43.14
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
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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 name
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IUPAC Traditional name
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MDL Number
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PubChem SID
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PubChem CID
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Product Information
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Physical Property
Related Proteins
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
007370
Apollo Scientific
PC9956
Key Organics
7P-057
Chemik
CHB54051
Enamine
EN300-91512
Bide Pharmatech
BD9753
Academic Data
PubChem
69699
Names and Identifiers
Synonyms
3-Bromo-4-fluoronitrobenzene
3-Bromo-4-fluoronitrobenzene
2-bromo-1-fluoro-4-nitrobenzene
3-Bromo-4-fluoro-1-nitrobenzene
IUPAC name
2-bromo-1-fluoro-4-nitrobenzene
IUPAC Traditional name
2-bromo-1-fluoro-4-nitrobenzene
Registration numbers
CAS Number
701-45-1
MDL Number
MFCD00055433
PubChem SID
160973854
PubChem CID
69699
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
Storage Warning
IRRITANT
Source
Irritant/Light Sensitive
Source
MSDS Link
Download link
Source
TSCA Listed
false
Source
Product Information
Purity
97%
Source
>95%
Source
95%
Source
Physical Property
>110°C
Source
55-58°C
Source
55 - 57 °C
Source
2.891
Source
Flash Point
Melting Point
Hydrophobicity(logP)