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Molecule
ID:92835
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₇BrN₂O
Molecular Mass
239.06868
Exact Mass
237.97417485
Charge
0
InChI
InChI=1S/C9H7BrN2O/c1-6-11-9(13-12-6)7-4-2-3-5-8(7)10/h2-5H,1H3
InChIKey
NYAFKUCVAVUCHW-UHFFFAOYSA-N
Canonic Smiles
Cc1noc(n1)c1ccccc1Br
Isomeric Smiles
o1c(nc(n1)C)c1ccccc1Br
Calculated Properties
JChem
H Acceptors
2
H Donor
0
LogD (pH = 5.5)
3.1287246
LogD (pH = 7.4)
3.128725
Log P
3.128725
Molar Refractivity
64.0229
Polarizability
20.311913
Polar Surface Area
38.92
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
•
RDKit
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JChem
Data Source
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Academic Data
Names and Identifiers
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IUPAC Traditional name
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Synonyms
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IUPAC name
Registration numbers
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CAS Number
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MDL Number
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PubChem SID
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PubChem CID
Properties
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Physical Property
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Safety Information
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Product Information
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
Apollo Scientific
OR9628
Maybridge
CC49610
Life Chemicals
F2145-0642
Enamine
EN300-79261
Academic Data
PubChem
18001310
Names and Identifiers
IUPAC Traditional name
5-(2-bromophenyl)-3-methyl-1,2,4-oxadiazole
Synonyms
5-(2-Bromophenyl)-3-methyl-1,2,4-oxadiazole 97%
5-(2-bromophenyl)-3-methyl-1,2,4-oxadiazole
IUPAC name
5-(2-bromophenyl)-3-methyl-1,2,4-oxadiazole
Registration numbers
CAS Number
375857-64-0
MDL Number
MFCD08435903
PubChem SID
162079533
PubChem CID
18001310
Properties
Physical Property
Melting Point
43-44°C
Source
Partition Coefficient
2.866
Source
Hydrophobicity(logP)
2.428
Source
Safety Information
Storage Warning
Irritant
Source
Product Information
Purity
97%
Source
95+%
Source
95%
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay