Details
Stereochemistry | ACHIRAL |
Molecular Formula | C7H15N |
Molecular Weight | 113.2007 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCN1CCCCC1
InChI
InChIKey=HTLZVHNRZJPSMI-UHFFFAOYSA-N
InChI=1S/C7H15N/c1-2-8-6-4-3-5-7-8/h2-7H2,1H3
Approval Year
PubMed
Title | Date | PubMed |
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A novel and efficient methodology for the C-C bond forming radical cyclization of hydrophobic substrates in water. | 2001 Apr 19 |
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Design, synthesis and biological evaluation of a novel series of potent, orally active adenosine A1 receptor antagonists with high blood-brain barrier permeability. | 2001 Aug |
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Triarylpyrazoles with basic side chains: development of pyrazole-based estrogen receptor antagonists. | 2001 Jan |
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Synthesis and structural studies of 1,1'-bis-amino-functionalized ferrocenes, ferrocene salts, and ferrocenium salts. | 2002 Feb 25 |
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Stereoselective synthesis of tetrasubstituted (Z)-alkenes from aryl alkyl ketones utilizing the Horner-Wadsworth-Emmons reaction. | 2002 Sep |
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Synthesis of 2',3'-dideoxyinosine via radical deoxygenation. | 2007 |
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DNA threading bis(9-aminoacridine-4-carboxamides): effects of piperidine sidechains on DNA binding, cytotoxicity and cell cycle arrest. | 2008 Apr 15 |
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Partial phenotypic reversion of ABA-deficient flacca tomato (Solanum lycopersicum) scions by a wild-type rootstock: normalizing shoot ethylene relations promotes leaf area but does not diminish whole plant transpiration rate. | 2009 |
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Binary complexes of tertiary amines with phenylacetylene. Dispersion wins over electrostatics. | 2010 Jun 21 |
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Design, synthesis, evaluation and QSAR analysis of N(1)-substituted norcymserine derivatives as selective butyrylcholinesterase inhibitors. | 2010 Mar 1 |
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C430119
Created by
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2090
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7IE43L0926
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39017
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766-09-6
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13007
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DTXSID1061102
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212-161-6
Created by
admin on Fri Dec 15 18:00:36 GMT 2023 , Edited by admin on Fri Dec 15 18:00:36 GMT 2023
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SUBSTANCE RECORD