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Molecule
ID:129843
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₉ClN₄S
Molecular Mass
252.72326
Exact Mass
252.02364499
Charge
0
InChI
InChI=1S/C10H9ClN4S/c11-9-2-1-8(5-13-9)6-15-3-4-16-10(15)14-7-12/h1-2,5H,3-4,6H2
InChIKey
HOKKPVIRMVDYPB-UHFFFAOYSA-N
Canonic Smiles
N#C/N=C\1/SCCN1Cc1ccc(nc1)Cl
Isomeric Smiles
Clc1ncc(cc1)CN1/C(=N\C#N)/SCC1
Calculated Properties
JChem
H Acceptors
4
H Donor
0
LogD (pH = 5.5)
2.0569935
LogD (pH = 7.4)
2.05705
Log P
2.0570507
Molar Refractivity
67.0453
Polarizability
24.672617
Polar Surface Area
52.28
Rotatable Bonds
2
Lipinski's Rule of Five
true
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Molecular Spectra
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Molecule Details
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Bioactivity
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General Information
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Thiacloprid
PubChem
115224
Names and Identifiers
IUPAC Traditional name
thiacloprid
Synonyms
Thiacloprid
[3-[(6-Chloro-3-pyridinyl)methyl]-2-thiazolidinylidene]cyanamide
IUPAC name
({3-[(6-chloropyridin-3-yl)methyl]-1,3-thiazolidin-2-ylidene}amino)carbonitrile
Registration numbers
CHEMBL
451432
Chemspider ID
103099
CHEBI ID
39176
KEGG ID
C18512
CAS Number
111988-49-9
Unique Ingredient Identifier
DSV3A944A4
Wikipedia Title
Thiacloprid
DrugBank ID
DB08620
PubChem CID
115224
PubChem SID
162224129
Properties
Physical Property
Melting Point
136°C
Source
Solubility
185 mg/L at 20°C in water
Source
Density
1.46 g·cm
-3
at 20 °C
Source
Apperance
Yellowish crystalline solid
Source
Molecule Details
Wikipedia
Thiacloprid
References
PubChem Literature
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Bioactivity
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CHEMBL
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Chemspider ID
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CHEBI ID
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KEGG ID
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CAS Number
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Unique Ingredient Identifier
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Wikipedia Title
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DrugBank ID
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PubChem CID
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PubChem SID