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=CC=CC2=C1C=CC=C2

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
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 Apr 18	11472119
Derivatization of ethinylestradiol with dansyl chloride to enhance electrospray ionization: application in trace analysis of ethinylestradiol in rhesus monkey plasma.	2002 Aug 15	12199585
Spectroscopic characterization of intramolecular charge transfer of sodium 4-(N,N-dimethylamino)naphthalene-1-sulfonate.	2004 Aug	15249007
Photoreactions between [60]fullerene and various aromatic tertiary amines.	2005 Oct 14	16209594
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 Jan 26	17142451
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 Aug 7	19525227
Species distribution and antimicrobial susceptibility of gram-negative aerobic bacteria in hospitalized cancer patients.	2009 Feb 19	19228413
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 Oct 30	20872635

Patents

Substance Class	Chemical Created by `admin` on `Sat Dec 16 04:14:52 GMT 2023` Edited by `admin` on `Sat Dec 16 04:14:52 GMT 2023`
Record UNII	020063I9Y0
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

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

NSC-8713

Code

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