U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C8H11N
Molecular Weight 121.1796
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,5-XYLIDINE

SMILES

CC1=CC(N)=C(C)C=C1

InChI

InChIKey=VOWZNBNDMFLQGM-UHFFFAOYSA-N
InChI=1S/C8H11N/c1-6-3-4-7(2)8(9)5-6/h3-5H,9H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C8H11N
Molecular Weight 121.1796
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Determination of the levels of aromatic amines in indoor and outdoor air in Italy.
2001 Apr
Characterization of a novel laccase produced by the wood-rotting fungus Phellinus ribis.
2001 Aug 15
Differential regulation of laccase gene expression in Pleurotus sajor-caju.
2001 Jul
Crystal structure of a four-copper laccase complexed with an arylamine: insights into substrate recognition and correlation with kinetics.
2002 Jun 11
[Dependence of activities of polysaccharide hydrolases and oxidases from Cerrena unicolor on the source of carbon and aromatic acids in culture media].
2002 May-Jun
Capture of a labile substrate by expulsion of water molecules from the active site of nicotinate mononucleotide:5,6-dimethylbenzimidazole phosphoribosyltransferase (CobT) from Salmonella enterica.
2002 Oct 25
Enzyme production by Mycena galopus mycelium in artificial media and in Picea sitchensis F1 horizon needle litter.
2003 Aug
Oligomeric compounds formed from 2,5-xylidine (2,5-dimethylaniline) are potent enhancers of laccase production in Trametes versicolor ATCC 32745.
2005 Aug
Prediction of genotoxicity of chemical compounds by statistical learning methods.
2005 Jun
Effects of culture conditions on production of extracellular laccase by Rhizoctonia praticola.
2006
Properties of laccases produced by Pycnoporus sanguineus induced by 2,5-xylidine.
2006 May
Production, purification and partial characterisation of a novel laccase from the white-rot fungus Panus tigrinus CBS 577.79.
2007 Jan
Laccase induction in fungi and laccase/N-OH mediator systems applied in paper mill effluent.
2007 Jan
Crystal structure of a blue laccase from Lentinus tigrinus: evidences for intermediates in the molecular oxygen reductive splitting by multicopper oxidases.
2007 Sep 26
A tannic acid-inducible and hypoviral-regulated Laccase3 contributes to the virulence of the chestnut blight fungus Cryphonectria parasitica.
2008 Dec
2,5-Dimethyl-anilinium chloride monohydrate.
2008 Dec 10
N-(2,5-Dimethyl-phen-yl)-4-methyl-benzene-sulfonamide.
2009 Dec 4
2,5-Dimethyl-anilinium nitrate.
2009 Jul 18
Bis(2,5-dimethyl-anilinium) tetra-chlorido-zincate(II).
2009 Mar 25
N-(2,5-Dimethyl-phen-yl)benzene-sulfonamide.
2009 Oct 17
Docking simulation and competitive experiments validate the interaction between the 2,5-xylidine inhibitor and Rigidoporus lignosus laccase.
2010 Feb
Heterologous expression of a tannic acid-inducible laccase3 of Cryphonectria parasitica in Saccharomyces cerevisiae.
2010 Feb 24
Differential volatile signatures from skin, naevi and melanoma: a novel approach to detect a pathological process.
2010 Nov 4
Fungal laccases: production, function, and applications in food processing.
2010 Sep 21
Two laccase isoenzymes and a peroxidase of a commercial laccase-producing basidiomycete, Trametes sp. Ha1.
2010 Sep 30
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 02:15:26 GMT 2023
Edited
by admin
on Sat Dec 16 02:15:26 GMT 2023
Record UNII
XWK0W8DA04
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,5-XYLIDINE
HSDB  
Systematic Name English
2,5-DIMETHYLANILINE
Systematic Name English
2,5-DIMETHYLBENZENAMINE
Systematic Name English
1-AMINO-2,5-DIMETHYLBENZENE
Systematic Name English
XYLIDINE 2,5-DIMETHYLBENZENAMINE
MI  
Systematic Name English
NSC-7639
Code English
BENZENAMINE, 2,5-DIMETHYL-
Systematic Name English
2,5-XYLIDINE [IARC]
Common Name English
2,5-XYLIDINE [HSDB]
Common Name English
XYLIDINE 2,5-DIMETHYLBENZENAMINE [MI]
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
202-451-0
Created by admin on Sat Dec 16 02:15:26 GMT 2023 , Edited by admin on Sat Dec 16 02:15:26 GMT 2023
PRIMARY
NSC
7639
Created by admin on Sat Dec 16 02:15:26 GMT 2023 , Edited by admin on Sat Dec 16 02:15:26 GMT 2023
PRIMARY
MERCK INDEX
m11552
Created by admin on Sat Dec 16 02:15:26 GMT 2023 , Edited by admin on Sat Dec 16 02:15:26 GMT 2023
PRIMARY Merck Index
WIKIPEDIA
2,5-XYLIDINE
Created by admin on Sat Dec 16 02:15:26 GMT 2023 , Edited by admin on Sat Dec 16 02:15:26 GMT 2023
PRIMARY
EPA CompTox
DTXSID3026306
Created by admin on Sat Dec 16 02:15:26 GMT 2023 , Edited by admin on Sat Dec 16 02:15:26 GMT 2023
PRIMARY
CAS
95-78-3
Created by admin on Sat Dec 16 02:15:26 GMT 2023 , Edited by admin on Sat Dec 16 02:15:26 GMT 2023
PRIMARY
PUBCHEM
7259
Created by admin on Sat Dec 16 02:15:26 GMT 2023 , Edited by admin on Sat Dec 16 02:15:26 GMT 2023
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DRUG BANK
DB02163
Created by admin on Sat Dec 16 02:15:26 GMT 2023 , Edited by admin on Sat Dec 16 02:15:26 GMT 2023
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FDA UNII
XWK0W8DA04
Created by admin on Sat Dec 16 02:15:26 GMT 2023 , Edited by admin on Sat Dec 16 02:15:26 GMT 2023
PRIMARY
HSDB
2093
Created by admin on Sat Dec 16 02:15:26 GMT 2023 , Edited by admin on Sat Dec 16 02:15:26 GMT 2023
PRIMARY
CHEBI
518305
Created by admin on Sat Dec 16 02:15:26 GMT 2023 , Edited by admin on Sat Dec 16 02:15:26 GMT 2023
PRIMARY