N,N-DIMETHYL-1-NAPHTHYLAMINE

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

Structure of N,N-DIMETHYL-1-NAPHTHYLAMINE

Structure Search

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

HIDE SMILES / InChI

Molecular Formula	C12H13N
Molecular Weight	171.2383
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
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	20872635
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	19525227
Species distribution and antimicrobial susceptibility of gram-negative aerobic bacteria in hospitalized cancer patients.	2009-02-19	19228413
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	17142451
Photoreactions between [60]fullerene and various aromatic tertiary amines.	2005-10-14	16209594
Spectroscopic characterization of intramolecular charge transfer of sodium 4-(N,N-dimethylamino)naphthalene-1-sulfonate.	2004-08	15249007
Derivatization of ethinylestradiol with dansyl chloride to enhance electrospray ionization: application in trace analysis of ethinylestradiol in rhesus monkey plasma.	2002-08-15	12199585
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	11472119

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:21:12 GMT 2025` Edited by `admin` on `Mon Mar 31 21:21:12 GMT 2025`
Record UNII	020063I9Y0
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

NSC-8713

Preferred Name

English

N,N-DIMETHYL-1-NAPHTHYLAMINE

Systematic Name

English

DIMETHYL(NAPHTH-1-YL)AMINE

Systematic Name

English

N,N-DIMETHYL-1-NAPHTHALENAMINE

Systematic Name

English

N,N-DIMETHYL-.ALPHA.-NAPHTHYLAMINE

Systematic Name

English

N,N-DIMETHYL-1-NAPHTHYLAMINE [MI]

Common Name

English

1-(DIMETHYLAMINO)NAPHTHALENE

Systematic Name

English

DIMETHYL-.ALPHA.-NAPHTHYLAMINE

Systematic Name

English

Code System Code Type Description

FDA UNII

020063I9Y0