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106983-30-6 molecular structure
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N-(2-oxooxolan-3-yl)octanamide

ChemBase ID: 156007
Molecular Formular: C12H21NO3
Molecular Mass: 227.30004
Monoisotopic Mass: 227.15214354
SMILES and InChIs

SMILES:
CCCCCCCC(=O)NC1CCOC1=O
Canonical SMILES:
CCCCCCCC(=O)NC1CCOC1=O
InChI:
InChI=1S/C12H21NO3/c1-2-3-4-5-6-7-11(14)13-10-8-9-16-12(10)15/h10H,2-9H2,1H3,(H,13,14)
InChIKey:
JKEJEOJPJVRHMQ-UHFFFAOYSA-N

Cite this record

CBID:156007 http://www.chembase.cn/molecule-156007.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
N-(2-oxooxolan-3-yl)octanamide
IUPAC Traditional name
N-(2-oxooxolan-3-yl)octanamide
Synonyms
N-Capryloyl-DL-homoserine lactone
N-Octanoyl-DL-homoserine lactone
CAS Number
106983-30-6
MDL Number
MFCD01862915
Beilstein Number
1642628
PubChem SID
162250145
24846914
PubChem CID
3474204

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID Price
Sigma Aldrich
10940 external link Add to cart Please log in.
Data Source Data ID
PubChem 3474204 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 12.706474  H Acceptors
H Donor LogD (pH = 5.5) 1.8410349 
LogD (pH = 7.4) 1.8410335  Log P 1.8410354 
Molar Refractivity 60.4899 cm3 Polarizability 24.098007 Å3
Polar Surface Area 55.4 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Safety Information Product Information Bioassay(PubChem)
MSDS Link
Download expand Show data source
German water hazard class
3 expand Show data source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand Show data source
Storage Temperature
2-8°C expand Show data source
Purity
≥97.0% (HPLC) expand Show data source
Empirical Formula (Hill Notation)
C12H21NO3 expand Show data source

DETAILS

DETAILS

Sigma Aldrich Sigma Aldrich
Sigma Aldrich - 10940 external link
Application
Application test: Induces violacein expression in a Chromobacterium violaceum mutant usually not able to produce homoserine lactones.1
Biochem/physiol Actions
N-Octanoyl-DL-homoserine lactone is a member of N-acyl-homoserine lactone family. N-acylhomoserine lactones (AHL) regulate gene expression in gram-negative bacteria, such as Echerichia and Salmonella are involved in quorum sensing, cell to cell communication among bacteria. Some AHLs are potent chemoattractants for human immune cells such as neutrophils.
N-octanoyl-homoserine lactone (N-C8-HSL) is among a group of homoserine lactones that includes; N-Heptanoyl-DL-homoserine lactone (C7HSL), N-Decanoyl-DL-homoserine lactone (N-C10-HSL), N-(3-oxodecanoyl) homoserine-L-lactone (3-oxo-C10 HSL), N-(3-oxododecanoyl)homoserine-L-lactone (3-oxo-C12-HSL), N-(3-Oxotetradecanoyl)-L-homoserine lactone (3-oxo-C14-HSL, N-(3-hydroxydecanoyl)-L-homoserine lactone, and N-(3-hydroxyoctanoyl)-L-homoserine lactone involved in the processes of bacterial quorum sensing. These N-acyl-homoserine lactones are used to study the processes and mechanisms of bacterial quorum sensing.

REFERENCES

REFERENCES

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PATENTS

PATENTS

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INTERNET

INTERNET

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