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Molecule
ID:15673
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₈N₂O
Molecular Mass
172.18332
Exact Mass
172.06366289
Charge
0
InChI
InChI=1S/C10H8N2O/c13-8-9-3-1-4-10(7-9)12-6-2-5-11-12/h1-8H
InChIKey
NKFXXJOWQSOGOF-UHFFFAOYSA-N
Canonic Smiles
O=Cc1cccc(c1)n1cccn1
Isomeric Smiles
n1(nccc1)c1cc(C=O)ccc1
Calculated Properties
JChem
H Acceptors
2
H Donor
0
LogD (pH = 5.5)
1.7715095
LogD (pH = 7.4)
1.7715659
Log P
1.7715666
Molar Refractivity
51.0037
Polarizability
19.303164
Polar Surface Area
34.89
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
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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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RDKit
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IUPAC Traditional name
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MDL Number
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PubChem CID
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Product Information
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Molecular Spectra
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
ChemBridge
4004821
Apollo Scientific
OR5681
Maybridge
CC32904
Key Organics
NA-0809
Matrix Scientific
016271
Enamine
EN300-75584
Academic Data
PubChem
7172309
Names and Identifiers
IUPAC Traditional name
3-(pyrazol-1-yl)benzaldehyde
Synonyms
3-(1H-Pyrazol-1-yl)benzaldehyde
3-(1H-Pyrazol-1-yl)benzenecarbaldehyde
IUPAC name
3-(1H-pyrazol-1-yl)benzaldehyde
Registration numbers
CAS Number
852227-92-0
MDL Number
MFCD06740321
PubChem CID
7172309
PubChem SID
160978980
Properties
Safety Information
MSDS Link
Download link
Source
Storage Warning
IRRITANT
Source
Harmful/Irritant
Source
TSCA Listed
false
Source
Physical Property
Melting Point
38-39°C
Source
79 - 81 °C
Source
Hydrophobicity(logP)
1.907
Source
Product Information
Purity
97%
Source
>95%
Source
95%
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay