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Molecule
ID:26073
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₅H₁₃FO₃
Molecular Mass
260.2603232
Exact Mass
260.0848725
Charge
0
InChI
InChI=1S/C15H13FO3/c1-18-15-8-12(9-17)4-7-14(15)19-10-11-2-5-13(16)6-3-11/h2-9H,10H2,1H3
InChIKey
PGCCPVWYLPJNBO-UHFFFAOYSA-N
Canonic Smiles
COc1cc(C=O)ccc1OCc1ccc(cc1)F
Isomeric Smiles
c1(c(OCc2ccc(F)cc2)ccc(c1)C=O)OC
Calculated Properties
JChem
H Acceptors
3
H Donor
0
LogD (pH = 5.5)
3.2375808
LogD (pH = 7.4)
3.2375808
Log P
3.2375808
Molar Refractivity
70.3974
Polarizability
26.517893
Polar Surface Area
35.53
Rotatable Bonds
5
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
Matrix Scientific
028622
Apollo Scientific
PC9333
Key Organics
1H-913
Enamine
EN300-01066
Academic Data
PubChem
737536
Names and Identifiers
Synonyms
4-(4-Fluorobenzyloxy)-3-methoxybenzaldehyde 97%
4-(4-Fluoro-benzyloxy)-3-methoxy-benzaldehyde
4-[(4-Fluorobenzyl)oxy]-3-methoxybenzenecarbaldehyde
IUPAC Traditional name
4-[(4-fluorophenyl)methoxy]-3-methoxybenzaldehyde
IUPAC name
4-[(4-fluorophenyl)methoxy]-3-methoxybenzaldehyde
Registration numbers
CAS Number
321432-05-7
MDL Number
MFCD00202628
PubChem CID
737536
PubChem SID
160989380
Properties
Safety Information
MSDS Link
Download link
Source
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
Irritant
Source
Physical Property
Melting Point
80-82°C
Source
80 - 82 °C
Source
78 - 80°C
Source
Hydrophobicity(logP)
3.361
Source
Product Information
Purity
>95%
Source
95%
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay