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Molecule
ID:40194
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₁H₉NO₃
Molecular Mass
203.19406
Exact Mass
203.05824315
Charge
0
InChI
InChI=1S/C11H9NO3/c1-14-11(13)9-7-10(15-12-9)8-5-3-2-4-6-8/h2-7H,1H3
InChIKey
XMPLCJOQBDGMKT-UHFFFAOYSA-N
Canonic Smiles
COC(=O)c1noc(c1)c1ccccc1
Isomeric Smiles
c1(noc(c1)c1ccccc1)C(=O)OC
Calculated Properties
JChem
H Acceptors
2
H Donor
0
LogD (pH = 5.5)
2.294345
LogD (pH = 7.4)
2.294345
Log P
2.094345
Molar Refractivity
54.167
Polarizability
21.698484
Polar Surface Area
52.33
Rotatable Bonds
3
Lipinski's Rule of Five
true
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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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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR15349
Key Organics
11Z-0717
Life Chemicals
F1727-0213
InterBioScreen
BB_SC-4984
STOCK1N-30587
Matrix Scientific
043176
Bide Pharmatech
BD105261
A&J Pharmtech
AJA-O5068
Academic Data
PubChem
905953
Names and Identifiers
Synonyms
Methyl 5-phenylisoxazole-3-carboxylate
Methyl 5-phenyl-3-isoxazolecarboxylate
IUPAC name
methyl 5-phenyl-1,2-oxazole-3-carboxylate
IUPAC Traditional name
methyl 5-phenyl-1,2-oxazole-3-carboxylate
Registration numbers
CAS Number
51677-09-9
MDL Number
MFCD02159553
PubChem SID
162044957
PubChem CID
905953
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Physical Property
Melting Point
82-84°C
Source
82 - 84 °C
Source
Partition Coefficient
2.276
Source
Product Information
Purity
>95%
Source
95+%
Source
97%
Source
Derivatives & analogs of Natural Compounds
Source
Safety Information
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Source
IRRITANT
Source
Irritant
Source
false
Source
Classification
MSDS Link
Storage Warning
TSCA Listed