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Molecule
ID:54309
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₇NO₂S
Molecular Mass
205.23308
Exact Mass
205.01974947
Charge
0
InChI
InChI=1S/C10H7NO2S/c12-10(13)8-6-11-9(14-8)7-4-2-1-3-5-7/h1-6H,(H,12,13)
InChIKey
LCALUFNLWHYTKX-UHFFFAOYSA-N
Canonic Smiles
OC(=O)c1cnc(s1)c1ccccc1
Isomeric Smiles
c1cccc(c1)c1sc(cn1)C(=O)O
Calculated Properties
JChem
Acid pKa
3.2304947
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
0.19333665
LogD (pH = 7.4)
-0.99404866
Log P
2.4468312
Molar Refractivity
63.4083
Polarizability
20.742254
Polar Surface Area
50.19
Rotatable Bonds
2
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
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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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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 CID
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PubChem SID
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Safety Information
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Product 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
Matrix Scientific
059223
Enamine
EN300-30651
Academic Data
PubChem
139087
Names and Identifiers
IUPAC Traditional name
2-phenyl-1,3-thiazole-5-carboxylic acid
Synonyms
2-Phenyl-thiazole-5-carboxylic acid
2-phenyl-1,3-thiazole-5-carboxylic acid
IUPAC name
2-phenyl-1,3-thiazole-5-carboxylic acid
Registration numbers
MDL Number
MFCD07376773
PubChem CID
139087
PubChem SID
162059072
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
MSDS Link
Download link
Source
Product Information
Purity
95+%
Source
95%
Source
Physical Property
187 - 189°C
Source
2.729
Source
Melting Point
Hydrophobicity(logP)