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Molecule
ID:99514
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₈F₃N₃
Molecular Mass
227.1858296
Exact Mass
227.06703193
Charge
0
InChI
InChI=1S/C10H8F3N3/c11-10(12,13)7-3-1-2-6-8(16-14)4-5-15-9(6)7/h1-5H,14H2,(H,15,16)
InChIKey
CJQJNVOPMJTCHC-UHFFFAOYSA-N
Canonic Smiles
NNc1ccnc2c1cccc2C(F)(F)F
Isomeric Smiles
n1ccc(c2cccc(c12)C(F)(F)F)NN
Calculated Properties
JChem
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
2.0949807
LogD (pH = 7.4)
2.3955426
Log P
2.4003916
Molar Refractivity
55.6597
Polarizability
20.51519
Polar Surface Area
50.94
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 name
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IUPAC Traditional name
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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
Apollo Scientific
PC7188
InterBioScreen
BB_SC-8632
Enamine
EN300-110530
A&J Pharmtech
AJA-O39686
Academic Data
PubChem
15151238
Names and Identifiers
Synonyms
4-Hydrazino-8-(trifluoromethyl)quinoline
4-hydrazinyl-8-(trifluoromethyl)quinoline
4-HYDRAZINO-8-TRIFLUOROMETHYL-QUINOLINE
IUPAC name
4-hydrazinyl-8-(trifluoromethyl)quinoline
IUPAC Traditional name
4-hydrazinyl-8-(trifluoromethyl)quinoline
Registration numbers
MDL Number
MFCD00272472
CAS Number
57369-92-3
PubChem SID
162085778
PubChem CID
15151238
Properties
Safety Information
Storage Warning
Irritant
Source
Physical Property
Hydrophobicity(logP)
3.179
Source
Product Information
Purity
95%
Source
98%
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay