Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H11NO |
| Molecular Weight | 113.1576 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=CN1CCCCC1
InChI
InChIKey=FEWLNYSYJNLUOO-UHFFFAOYSA-N
InChI=1S/C6H11NO/c8-6-7-4-2-1-3-5-7/h6H,1-5H2
| Molecular Formula | C6H11NO |
| Molecular Weight | 113.1576 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Highly stereoselective asymmetric Pummerer reactions that incorporate intermolecular and intramolecular nonbonded S...O interactions. | 2006-08-02 |
|
| Regio- and chemoselective direct generation of functionalized aromatic aluminum compounds using aluminum ate base. | 2004-09-01 |
|
| Ketone enolization with lithium dialkylamides: the effects of structure, solvation, and mixed aggregates with excess butyllithium. | 2003-08-08 |
|
| Synthesis and biological evaluation of novel carbon-11-labelled analogues of citalopram as potential radioligands for the serotonin transporter. | 2003-08-05 |
|
| Molecular markers of anthropogenic activity in sediments of the Havel and Spree Rivers (Germany). | 2003-06 |
|
| Synthesis and muscarinic M2 subtype antagonistic activity of unnatural ent-himbacine and an enantiomeric pair of (2'S,6'R)-diepihimbacine. | 2002-10-21 |
|
| Structure activity relationship by NMR and by computer: a comparative study. | 2002-09-18 |
|
| Transport of peptidomimetic thrombin inhibitors with a 3-amidino-phenylalanine structure: permeability and efflux mechanism in monolayers of a human intestinal cell line (Caco-2). | 2001-08 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:57:49 GMT 2025
by
admin
on
Mon Mar 31 21:57:49 GMT 2025
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| Record UNII |
ZIQ29H6CZG
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| Record Status |
Validated (UNII)
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| Record Version |
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17429
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DTXSID8043941
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404158
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219-986-0
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DB04113
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N-Formylpiperidine
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