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Molecule
ID:117715
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₁₃NO₄
Molecular Mass
187.19312
Exact Mass
187.0844579
Charge
0
InChI
InChI=1S/C8H13NO4/c1-13-8(12)9-4-2-3-6(5-9)7(10)11/h6H,2-5H2,1H3,(H,10,11)
InChIKey
JUWHQANQIXFDDM-UHFFFAOYSA-N
Canonic Smiles
COC(=O)N1CCCC(C1)C(=O)O
Isomeric Smiles
N1(C(=O)OC)CC(C(=O)O)CCC1
Calculated Properties
JChem
Acid pKa
4.2144294
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
-1.0396657
LogD (pH = 7.4)
-2.7582135
Log P
0.26537305
Molar Refractivity
44.1108
Polarizability
17.295618
Polar Surface Area
66.84
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
Calculated Properties
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RDKit
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Synonyms
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IUPAC name
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IUPAC Traditional name
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MDL Number
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PubChem SID
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PubChem CID
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Physical Property
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Product Information
Related Proteins
Molecular Spectra
Molecule Details
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Life Chemicals
F2158-1183
Enamine
EN300-69787
Academic Data
PubChem
20598064
Names and Identifiers
Synonyms
1-(methoxycarbonyl)piperidine-3-carboxylic acid
IUPAC name
1-(methoxycarbonyl)piperidine-3-carboxylic acid
IUPAC Traditional name
1-(methoxycarbonyl)piperidine-3-carboxylic acid
Registration numbers
MDL Number
MFCD11128996
PubChem SID
162091104
PubChem CID
20598064
Properties
Physical Property
Partition Coefficient
0.0080
Source
Hydrophobicity(logP)
0.809
Source
Product Information
Purity
95+%
Source
95%
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay