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Molecule
ID:10358
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₅H₇ClN₂O₂S
Molecular Mass
194.63928
Exact Mass
193.99167615
Charge
0
InChI
InChI=1S/C5H7ClN2O2S/c1-4-7-5(3-8(4)2)11(6,9)10/h3H,1-2H3
InChIKey
JPAFTHVNSBWVQJ-UHFFFAOYSA-N
Canonic Smiles
Cn1cc(nc1C)S(=O)(=O)Cl
Isomeric Smiles
n1(c(nc(c1)S(=O)(=O)Cl)C)C
Calculated Properties
JChem
H Acceptors
3
H Donor
0
LogD (pH = 5.5)
0.74225926
LogD (pH = 7.4)
0.7422769
Log P
0.74227715
Molar Refractivity
42.8579
Polarizability
16.886143
Polar Surface Area
51.96
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
No Data Available
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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
•
JChem
Data Source
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Commercial Catalog
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Academic Data
Names and Identifiers
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IUPAC Traditional name
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IUPAC name
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Synonyms
Registration numbers
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MDL Number
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CAS Number
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PubChem SID
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PubChem CID
Properties
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Product Information
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Safety Information
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Physical Property
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
OR0412
Matrix Scientific
007142
Maybridge
KM10104
InterBioScreen
BB_SC-2496
Enamine
EN300-58948
Academic Data
PubChem
2736256
Names and Identifiers
IUPAC Traditional name
1,2-dimethylimidazole-4-sulfonyl chloride
IUPAC name
1,2-dimethyl-1H-imidazole-4-sulfonyl chloride
Synonyms
1,2-Dimethylimidazole-4-sulfonyl chloride
1,2-dimethyl-1H-imidazole-4-sulfonyl chloride
1,2-Dimethyl-1H-imidazole-4-sulphonyl chloride 95%
Registration numbers
MDL Number
MFCD01313780
CAS Number
137049-02-6
PubChem SID
160973665
PubChem CID
2736256
Properties
Product Information
Purity
95+%
Source
95%
Source
Safety Information
Storage Warning
MOISTURE SENSITIVE, CORROSIVE
Source
Corrosive/Store under Argon
Source
MSDS Link
Download link
Source
TSCA Listed
false
Source
Physical Property
Melting Point
91-94°C
Source
91-94°C°C
Source
91 - 93°C
Source
Hydrophobicity(logP)
-1.716
Source
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay