Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H13N |
| Molecular Weight | 171.2383 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CN(C)C1=C2C=CC=CC2=CC=C1
InChI
InChIKey=AJUXDFHPVZQOGF-UHFFFAOYSA-N
InChI=1S/C12H13N/c1-13(2)12-9-5-7-10-6-3-4-8-11(10)12/h3-9H,1-2H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Dansyl-peptides matrix-assisted laser desorption/ionization mass spectrometric (MALDI-MS) and tandem mass spectrometric (MS/MS) features improve the liquid chromatography/MALDI-MS/MS analysis of the proteome. | 2010-10-30 |
|
| Biosynthesis and structure of the Burkholderia cenocepacia K56-2 lipopolysaccharide core oligosaccharide: truncation of the core oligosaccharide leads to increased binding and sensitivity to polymyxin B. | 2009-08-07 |
|
| Species distribution and antimicrobial susceptibility of gram-negative aerobic bacteria in hospitalized cancer patients. | 2009-02-19 |
|
| Serine and cysteine proteases are translocated to similar extents upon formation of covalent complexes with serpins. Fluorescence perturbation and fluorescence resonance energy transfer mapping of the protease binding site in CrmA complexes with granzyme B and caspase-1. | 2007-01-26 |
|
| Photoreactions between [60]fullerene and various aromatic tertiary amines. | 2005-10-14 |
|
| Spectroscopic characterization of intramolecular charge transfer of sodium 4-(N,N-dimethylamino)naphthalene-1-sulfonate. | 2004-08 |
|
| Derivatization of ethinylestradiol with dansyl chloride to enhance electrospray ionization: application in trace analysis of ethinylestradiol in rhesus monkey plasma. | 2002-08-15 |
|
| Use of aromatic radical-anions in the absence of THF. Tandem formation and cyclization of benzyllithiums derived from the attack of homo- and bishomoallyllithiums on alpha-methylstyrenes: two-pot synthesis of cuparene. | 2001-04-18 |
Patents
| Name | Type | Language | ||
|---|---|---|---|---|
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Preferred Name | English | ||
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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020063I9Y0
Created by
admin on Mon Mar 31 21:21:12 GMT 2025 , Edited by admin on Mon Mar 31 21:21:12 GMT 2025
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N,N-DIMETHYL-1-NAPHTHYLAMINE
Created by
admin on Mon Mar 31 21:21:12 GMT 2025 , Edited by admin on Mon Mar 31 21:21:12 GMT 2025
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C034361
Created by
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201-682-4
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6848
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86-56-6
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8713
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m4546
Created by
admin on Mon Mar 31 21:21:12 GMT 2025 , Edited by admin on Mon Mar 31 21:21:12 GMT 2025
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PRIMARY | Merck Index | ||
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DTXSID9058941
Created by
admin on Mon Mar 31 21:21:12 GMT 2025 , Edited by admin on Mon Mar 31 21:21:12 GMT 2025
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PRIMARY |
SUBSTANCE RECORD
