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Molecule
ID:43535
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₄BrN₃O₂
Molecular Mass
242.02956
Exact Mass
240.94868838
Charge
0
InChI
InChI=1S/C7H4BrN3O2/c8-7-5-3-4(11(12)13)1-2-6(5)9-10-7/h1-3H,(H,9,10)
InChIKey
SYTGRKBQTUKOAI-UHFFFAOYSA-N
Canonic Smiles
[O-][N+](=O)c1cc2c(Br)n[nH]c2cc1
Isomeric Smiles
c1(ccc2c(c1)c(n[nH]2)Br)[N+](=O)[O-]
Calculated Properties
JChem
Acid pKa
8.889426
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
2.2103937
LogD (pH = 7.4)
2.1970615
Log P
2.2105665
Molar Refractivity
50.8586
Polarizability
19.485662
Polar Surface Area
71.82
Rotatable Bonds
1
Lipinski's Rule of Five
true
Data Source
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Names and Identifiers
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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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IUPAC name
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IUPAC Traditional name
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Product Information
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Physical Property
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Molecular Spectra
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR12046
Matrix Scientific
046878
Key Organics
EA-0849
Bide Pharmatech
BD105016
A&J Pharmtech
AJA-O29270
Academic Data
PubChem
640614
Names and Identifiers
IUPAC name
3-bromo-5-nitro-1H-indazole
Synonyms
3-Bromo-5-nitro-1H-indazole
3-Bromo-5-nitroindazole
5-NITRO-3-BROMOINDAZOLE
IUPAC Traditional name
3-bromo-5-nitro-1H-indazole
Registration numbers
PubChem SID
162048298
PubChem CID
640614
MDL Number
MFCD07367964
CAS Number
67400-25-3
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
MSDS Link
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Source
Storage Warning
IRRITANT
Source
Irritant
Source
TSCA Listed
false
Source
Product Information
Purity
>95%
Source
95+%
Source
98%
Source
Physical Property
227-229°C
Source
227 - 229 °C
Source
Melting Point