Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H9NO |
| Molecular Weight | 159.1846 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=C(O)C2=CC=CC=C2C=C1
InChI
InChIKey=QPKNFEVLZVJGBM-UHFFFAOYSA-N
InChI=1S/C10H9NO/c11-9-6-5-7-3-1-2-4-8(7)10(9)12/h1-6,12H,11H2
| Molecular Formula | C10H9NO |
| Molecular Weight | 159.1846 |
| 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 |
|---|---|---|
| High-performance liquid chromatographic enantioseparation of aminonaphthol analogs on polysaccharide-based chiral stationary phases. | 2010-04-23 |
|
| Characterization of indigenous Rhodococcus sp. 602, a strain able to accumulate triacylglycerides from naphthyl compounds under nitrogen-starved conditions. | 2010-04 |
|
| Microwave-assisted synthesis of 2'-O-aryluridine derivatives. | 2009-12-17 |
|
| 5-Amino-1-naphthol. | 2009-10-31 |
|
| Degradation analysis of Reactive Red 198 by hairy roots of Tagetes patula L. (Marigold). | 2009-09 |
|
| A novel iron-catalyzed decarboxylative Csp3-Csp2 coupling of proline derivatives and naphthol. | 2009-08-06 |
|
| Synthesis and biological evaluation of a novel pentagastrin-toxin conjugate designed for a targeted prodrug mono-therapy of cancer. | 2008-05 |
|
| Novel fluorescent sensor for detection of Cu(II) in aqueous solution. | 2006-11 |
|
| New fluorescent chemosensor based on exciplex signaling mechanism. | 2005-05-26 |
|
| Highly enantioselective phenyl transfer to aryl aldehydes catalyzed by easily accessible chiral tertiary aminonaphthol. | 2005-02-04 |
|
| Torsional barriers in aromatic molecular clusters as probe of the electronic properties of the chromophore. | 2004-11-12 |
|
| Time-resolved photoionisation of radicals, clusters and biomolecules: relevant model systems. | 2003-03 |
|
| A convenient, one-step synthesis of optically active tertiary aminonaphthol and its applications in the highly enantioselective alkenylations of aldehydes. | 2003-02-21 |
|
| The application of chiral aminonaphthols in the enantioselective addition of diethylzinc to aryl aldehydes. | 2001-08-23 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:36:08 GMT 2025
by
admin
on
Mon Mar 31 19:36:08 GMT 2025
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| Record UNII |
797L65QKKD
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| Record Status |
Validated (UNII)
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| Record Version |
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DTXSID10209406
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797L65QKKD
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39038
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606-41-7
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210-117-0
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C035914
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