Details
Stereochemistry | ACHIRAL |
Molecular Formula | C7H15NO |
Molecular Weight | 129.2001 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OCCN1CCCCC1
InChI
InChIKey=KZTWONRVIPPDKH-UHFFFAOYSA-N
InChI=1S/C7H15NO/c9-7-6-8-4-2-1-3-5-8/h9H,1-7H2
Molecular Formula | C7H15NO |
Molecular Weight | 129.2001 |
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 |
---|---|---|
Triarylpyrazoles with basic side chains: development of pyrazole-based estrogen receptor antagonists. | 2001 Jan |
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Indolizino[1,2-b]quinolines derived from A-D rings of camptothecin: synthesis and DNA interaction. | 2003 Apr |
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N-hydroxyethyl-piperidine and -pyrrolidine homoazasugars: preparation and evaluation of glycosidase inhibitory activity. | 2003 Jul 31 |
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Stereospecific rearrangements during the synthesis of pyrrolidines and related heterocycles from cyclizations of amino alcohols with vinyl Sulfones. | 2003 Nov 28 |
|
Studies toward labeling cytisine with [11C]phosgene: rapid synthesis of a delta-lactam involving a new chemoselective lithiation-annulation method. | 2004 May 28 |
|
Synthesis of an optically pure synthetic intermediate of aloperine from a yeast-reductive product. | 2005 Aug |
|
The enhancing effect of ion-pairing on the skin permeation of glipizide. | 2009 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:24:28 GMT 2023
by
admin
on
Fri Dec 15 16:24:28 GMT 2023
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Record UNII |
VR81F07RX5
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Record Status |
Validated (UNII)
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Record Version |
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