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Molecule
ID:43998
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₉NO₂S
Molecular Mass
171.21686
Exact Mass
171.03539953
Charge
0
InChI
InChI=1S/C7H9NO2S/c1-3-10-7(9)6-5(2)8-4-11-6/h4H,3H2,1-2H3
InChIKey
WISQBJLUORKXNY-UHFFFAOYSA-N
Canonic Smiles
CCOC(=O)c1scnc1C
Isomeric Smiles
c1(c(ncs1)C)C(=O)OCC
Calculated Properties
JChem
H Acceptors
2
H Donor
0
LogD (pH = 5.5)
1.2561294
LogD (pH = 7.4)
1.2561331
Log P
1.2561331
Molar Refractivity
42.4159
Polarizability
16.223648
Polar Surface Area
39.19
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
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
•
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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Synonyms
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IUPAC name
Registration numbers
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MDL Number
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CAS Number
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PubChem CID
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PubChem SID
Properties
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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
Apollo Scientific
OR40519
Matrix Scientific
047379
Key Organics
GC-0751
Enamine
EN300-64741
Academic Data
PubChem
298610
Names and Identifiers
IUPAC Traditional name
ethyl 4-methyl-1,3-thiazole-5-carboxylate
Synonyms
Ethyl 4-methyl-1,3-thiazole-5-carboxylate
5-(Ethoxycarbonyl)-4-methyl-1,3-thiazole
IUPAC name
ethyl 4-methyl-1,3-thiazole-5-carboxylate
Registration numbers
MDL Number
MFCD00626873
CAS Number
20582-55-2
PubChem CID
298610
PubChem SID
162048761
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
MSDS Link
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Source
Storage Warning
IRRITANT
Source
Harmful/Irritant/Keep Cold
Source
TSCA Listed
false
Source
Product Information
Purity
95+%
Source
>95%
Source
95%
Source
Physical Property
Oil
Source
1.605
Source
Melting Point
Hydrophobicity(logP)