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Molecule
ID:75446
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₃BrN₂O₂
Molecular Mass
227.01492
Exact Mass
225.93778935
Charge
0
InChI
InChI=1S/C7H3BrN2O2/c8-7-2-1-6(10(11)12)3-5(7)4-9/h1-3H
InChIKey
RKODNVITKISFKU-UHFFFAOYSA-N
Canonic Smiles
N#Cc1cc(ccc1Br)[N+](=O)[O-]
Isomeric Smiles
N#Cc1c(ccc(c1)[N+](=O)[O-])Br
Calculated Properties
JChem
H Acceptors
3
H Donor
0
LogD (pH = 5.5)
2.5380788
LogD (pH = 7.4)
2.5380788
Log P
2.5380788
Molar Refractivity
45.7229
Polarizability
17.066212
Polar Surface Area
66.93
Rotatable Bonds
1
Lipinski's Rule of Five
true
Data Source
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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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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR11410
Sigma Aldrich
701238
Chemik
CHB27324
A&J Pharmtech
AJA-O620
Academic Data
PubChem
7095423
Names and Identifiers
Synonyms
2-Bromo-5-nitrobenzonitrile 98%
2-Bromo-1-cyano-5-nitrobenzene
2-溴-5-硝基苯甲腈
2-Bromo-5-nitrobenzonitrile
2-bromo-5-nitrobenzonitrile
1-Cyano-2-broMo-5-nitrobenzene
IUPAC Traditional name
2-bromo-5-nitrobenzonitrile
IUPAC name
2-bromo-5-nitrobenzonitrile
Registration numbers
MDL Number
MFCD00234249
CAS Number
134604-07-2
PubChem SID
162040364
PubChem CID
7095423
Molecule Details
Sigma Aldrich
701238
Packaging
5 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
Storage Warning
Irritant/Store under Argon/Moisture Sensitive
Source
Storage Temperature
2-8°C
Source
MSDS Link
Download link
Source
German water hazard class
3
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
Product Information
97%
Source
98%
Source
C7H3BrN2O2
Source
Physical Property
118-120 °C
Source
Purity
Empirical Formula (Hill Notation)
Melting Point