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=CC=C2C=CC=CC2=C1O
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 |
|---|---|---|
| A convenient, one-step synthesis of optically active tertiary aminonaphthol and its applications in the highly enantioselective alkenylations of aldehydes. | 2003 Feb 21 |
|
| Torsional barriers in aromatic molecular clusters as probe of the electronic properties of the chromophore. | 2004 Nov 12 |
|
| Microwave-assisted synthesis of 2'-O-aryluridine derivatives. | 2009 Dec 17 |
|
| 5-Amino-1-naphthol. | 2009 Oct 31 |
|
| Degradation analysis of Reactive Red 198 by hairy roots of Tagetes patula L. (Marigold). | 2009 Sep |
|
| Characterization of indigenous Rhodococcus sp. 602, a strain able to accumulate triacylglycerides from naphthyl compounds under nitrogen-starved conditions. | 2010 Apr |
|
| High-performance liquid chromatographic enantioseparation of aminonaphthol analogs on polysaccharide-based chiral stationary phases. | 2010 Apr 23 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:12:23 GMT 2023
by
admin
on
Fri Dec 15 19:12:23 GMT 2023
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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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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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