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=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
Approval Year
PubMed
Title | Date | PubMed |
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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 |
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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 |
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Species distribution and antimicrobial susceptibility of gram-negative aerobic bacteria in hospitalized cancer patients. | 2009 Feb 19 |
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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 |
Patents
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020063I9Y0
Created by
admin on Sat Dec 16 04:14:52 GMT 2023 , Edited by admin on Sat Dec 16 04:14:52 GMT 2023
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N,N-DIMETHYL-1-NAPHTHYLAMINE
Created by
admin on Sat Dec 16 04:14:52 GMT 2023 , Edited by admin on Sat Dec 16 04:14:52 GMT 2023
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C034361
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201-682-4
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6848
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86-56-6
Created by
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8713
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m4546
Created by
admin on Sat Dec 16 04:14:52 GMT 2023 , Edited by admin on Sat Dec 16 04:14:52 GMT 2023
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DTXSID9058941
Created by
admin on Sat Dec 16 04:14:52 GMT 2023 , Edited by admin on Sat Dec 16 04:14:52 GMT 2023
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SUBSTANCE RECORD