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Molecule
ID:14928
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₁H₁₂N₂O₂S
Molecular Mass
236.29018
Exact Mass
236.06194863
Charge
0
InChI
InChI=1S/C11H12N2O2S/c1-14-9-4-3-7(5-10(9)15-2)8-6-16-11(12)13-8/h3-6H,1-2H3,(H2,12,13)
InChIKey
QNLNRENPKAQTMJ-UHFFFAOYSA-N
Canonic Smiles
COc1cc(ccc1OC)c1csc(n1)N
Isomeric Smiles
c1(c2csc(n2)N)cc(c(cc1)OC)OC
Calculated Properties
JChem
Acid pKa
16.702074
H Acceptors
4
H Donor
1
LogD (pH = 5.5)
2.1897025
LogD (pH = 7.4)
2.2048984
Log P
2.2050958
Molar Refractivity
63.1307
Polarizability
25.212326
Polar Surface Area
57.37
Rotatable Bonds
3
Lipinski's Rule of Five
true
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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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From Data Sources
Bioactivity
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Data Source
Commercial Catalog
Matrix Scientific
012472
Life Chemicals
F1386-0384
InterBioScreen
BB_SC-9571
ChemBridge
6872713
Enamine
EN300-02232
Academic Data
PubChem
332397
Names and Identifiers
IUPAC Traditional name
4-(3,4-dimethoxyphenyl)-1,3-thiazol-2-amine
Synonyms
4-(3,4-Dimethoxy-phenyl)-thiazol-2-ylamine
4-(3,4-dimethoxyphenyl)-1,3-thiazol-2-amine
4-(3,4-dimethoxyphenyl)thiazol-2-amine
IUPAC name
4-(3,4-dimethoxyphenyl)-1,3-thiazol-2-amine
Registration numbers
MDL Number
MFCD01088726
CAS Number
51837-85-5
PubChem SID
160978235
PubChem CID
332397
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
Storage Warning
IRRITANT
Source
MSDS Link
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Source
TSCA Listed
false
Source
Physical Property
Partition Coefficient
1.78674
Source
Hydrophobicity(logP)
2.062
Source
Product Information
95+%
Source
95%
Source
Purity