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Molecule
ID:63191
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₄H₁₇NO
Molecular Mass
215.29088
Exact Mass
215.13101417
Charge
0
InChI
InChI=1S/C14H17NO/c16-14-8-12-6-7-13(9-14)15(12)10-11-4-2-1-3-5-11/h1-5,12-13H,6-10H2/t12-,13+
InChIKey
RSUHKGOVXMXCND-BETUJISGSA-N
Canonic Smiles
O=C1C[C@@H]2CC[C@H](C1)N2Cc1ccccc1
Isomeric Smiles
N1(Cc2ccccc2)[C@H]2CC[C@@H]1CC(=O)C2
Calculated Properties
JChem
Acid pKa
18.179075
H Acceptors
2
H Donor
0
LogD (pH = 5.5)
-0.61108047
LogD (pH = 7.4)
1.0905402
Log P
2.4229376
Molar Refractivity
63.9575
Polarizability
25.213005
Polar Surface Area
20.31
Rotatable Bonds
2
Lipinski's Rule of Five
true
Data Source
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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
Calculated Properties
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RDKit
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JChem
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IUPAC Traditional name
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IUPAC name
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PubChem CID
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CAS Number
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MDL Number
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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
Matrix Scientific
068505
Chemik
CHB85771
Enamine
EN300-123987
Academic Data
PubChem
11183512
Names and Identifiers
IUPAC Traditional name
(1R,5S)-8-benzyl-8-azabicyclo[3.2.1]octan-3-one
Synonyms
(1R,5S)-8-Benzyl-8-azabicyclo[3.2.1]octan-3-one
N-benzylnortropinone
IUPAC name
(1R,5S)-8-benzyl-8-azabicyclo[3.2.1]octan-3-one
Registration numbers
PubChem SID
162028930
PubChem CID
11183512
CAS Number
28957-72-4
MDL Number
MFCD00151640
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
MSDS Link
Download link
Source
Product Information
Purity
>95%
Source
95%
Source
Physical Property
2.14
Source
Hydrophobicity(logP)