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Molecule
ID:114918
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₁₇NO₂
Molecular Mass
171.23678
Exact Mass
171.12592879
Charge
0
InChI
InChI=1S/C9H17NO2/c1-8(9(11)12)7-10-5-3-2-4-6-10/h8H,2-7H2,1H3,(H,11,12)
InChIKey
FNXJEHJSDJHSFC-UHFFFAOYSA-N
Canonic Smiles
CC(C(=O)O)CN1CCCCC1
Isomeric Smiles
C(C(=O)O)(CN1CCCCC1)C
Calculated Properties
JChem
Acid pKa
3.944929
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
-1.441638
LogD (pH = 7.4)
-1.4324584
Log P
-1.4322948
Molar Refractivity
47.4886
Polarizability
18.621471
Polar Surface Area
40.54
Rotatable Bonds
3
Lipinski's Rule of Five
true
Data Source
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Names and Identifiers
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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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CAS Number
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PubChem CID
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PubChem SID
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Product Information
Related Proteins
Molecular Spectra
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
ChemBridge
4027837
Life Chemicals
F2130-0025
Enamine
EN300-58036
Academic Data
PubChem
4739598
Names and Identifiers
IUPAC name
2-methyl-3-(piperidin-1-yl)propanoic acid
Synonyms
2-methyl-3-(1-piperidinyl)propanoic acid
2-Methyl-3-piperidin-1-ylpropanoic acid hydrochloride
2-methyl-3-(piperidin-1-yl)propanoic acid
IUPAC Traditional name
2-methyl-3-(piperidin-1-yl)propanoic acid
Registration numbers
MDL Number
MFCD07211808
MFCD06255269
CAS Number
24007-12-3
PubChem CID
4739598
PubChem SID
162101090
Properties
Physical Property
Partition Coefficient
1.104
Source
Hydrophobicity(logP)
-0.716
Source
Product Information
Purity
95+%
Source
95%
Source
Salt Data
HCl
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay