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Molecule
ID:45789
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₁₇NO₃
Molecular Mass
199.24688
Exact Mass
199.12084341
Charge
0
InChI
InChI=1S/C10H17NO3/c1-7(2)9(12)11-5-3-8(4-6-11)10(13)14/h7-8H,3-6H2,1-2H3,(H,13,14)
InChIKey
BNSWWHNOGGYQAN-UHFFFAOYSA-N
Canonic Smiles
CC(C(=O)N1CCC(CC1)C(=O)O)C
Isomeric Smiles
N1(C(=O)C(C)C)CCC(C(=O)O)CC1
Calculated Properties
JChem
Acid pKa
4.5885186
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
-0.22697942
LogD (pH = 7.4)
-2.0023966
Log P
0.7336966
Molar Refractivity
51.8426
Polarizability
20.189966
Polar Surface Area
57.61
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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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
4031473
Matrix Scientific
049273
Enamine
EN300-28872
Academic Data
PubChem
16770959
Names and Identifiers
IUPAC Traditional name
1-(2-methylpropanoyl)piperidine-4-carboxylic acid
Synonyms
1-Isobutyryl-4-piperidinecarboxylic acid
1-isobutyrylpiperidine-4-carboxylic acid
IUPAC name
1-(2-methylpropanoyl)piperidine-4-carboxylic acid
Registration numbers
MDL Number
MFCD09043253
CAS Number
330985-26-7
PubChem CID
16770959
PubChem SID
162050552
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
MSDS Link
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Source
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
Physical Property
Hydrophobicity(logP)
-0.698
Source
Melting Point
102 - 104°C
Source
Product Information
95%
Source
Purity