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Molecule
ID:40364
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₅Cl₃N₂O
Molecular Mass
263.5078
Exact Mass
261.94674583
Charge
0
InChI
InChI=1S/C9H5Cl3N2O/c10-4-8-13-14-9(15-8)6-2-1-5(11)3-7(6)12/h1-3H,4H2
InChIKey
PRFJGLYRTYUAFU-UHFFFAOYSA-N
Canonic Smiles
ClCc1nnc(o1)c1ccc(cc1Cl)Cl
Isomeric Smiles
c1(nnc(o1)CCl)c1c(cc(cc1)Cl)Cl
Calculated Properties
JChem
H Acceptors
2
H Donor
0
LogD (pH = 5.5)
2.8479536
LogD (pH = 7.4)
2.8479538
Log P
2.8479538
Molar Refractivity
70.8887
Polarizability
23.284882
Polar Surface Area
38.92
Rotatable Bonds
2
Lipinski's Rule of Five
true
Data Source
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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
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Product Information
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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
OR9843
Key Organics
12Y-0810
Matrix Scientific
043372
Enamine
EN300-54045
Academic Data
PubChem
2763460
Names and Identifiers
IUPAC name
2-(chloromethyl)-5-(2,4-dichlorophenyl)-1,3,4-oxadiazole
IUPAC Traditional name
2-(chloromethyl)-5-(2,4-dichlorophenyl)-1,3,4-oxadiazole
Synonyms
2-(Chloromethyl)-5-(2,4-dichlorophenyl)-1,3,4-oxadiazole
2-Chloromethyl-5-(2,4-dichlorophenyl)-1,3,4-oxadiazole
Registration numbers
PubChem CID
2763460
PubChem SID
162045127
MDL Number
MFCD06797383
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Physical Property
Melting Point
85-87°C
Source
85 - 87 °C
Source
87 - 89°C
Source
Hydrophobicity(logP)
2.463
Source
Safety Information
MSDS Link
Download link
Source
IRRITANT
Source
false
Source
Product Information
>95%
Source
95%
Source
Storage Warning
TSCA Listed
Purity