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Molecule
ID:116880
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₁H₁₂ClNO₃
Molecular Mass
241.67088
Exact Mass
241.05057093
Charge
0
InChI
InChI=1S/C11H12ClNO3/c1-15-9-4-2-8(3-5-9)13-7-10(6-12)16-11(13)14/h2-5,10H,6-7H2,1H3
InChIKey
YHJWPLPRXWMHBK-UHFFFAOYSA-N
Canonic Smiles
ClCC1CN(C(=O)O1)c1ccc(cc1)OC
Isomeric Smiles
C1(=O)N(c2ccc(cc2)OC)CC(O1)CCl
Calculated Properties
JChem
H Acceptors
3
H Donor
0
LogD (pH = 5.5)
2.089374
LogD (pH = 7.4)
2.089374
Log P
2.089374
Molar Refractivity
59.1682
Polarizability
23.25976
Polar Surface Area
38.77
Rotatable Bonds
3
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
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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
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RDKit
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JChem
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Names and Identifiers
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IUPAC Traditional name
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Synonyms
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IUPAC name
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MDL Number
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PubChem SID
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PubChem CID
Properties
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Product Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Academic Data
PubChem
14368940
Commercial Catalog
Life Chemicals
F2147-0699
Names and Identifiers
IUPAC Traditional name
5-(chloromethyl)-3-(4-methoxyphenyl)-1,3-oxazolidin-2-one
Synonyms
5-(chloromethyl)-3-(4-methoxyphenyl)-1,3-oxazolidin-2-one
IUPAC name
5-(chloromethyl)-3-(4-methoxyphenyl)-1,3-oxazolidin-2-one
Registration numbers
MDL Number
MFCD16631775
PubChem SID
162101880
PubChem CID
14368940
Properties
Product Information
Purity
95+%
Source
Physical Property
Partition Coefficient
1.959
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay