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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 2,3-XYLIDINE

SMILES

CC1=CC=CC(N)=C1C

InChI

InChIKey=VVAKEQGKZNKUSU-UHFFFAOYSA-N
InChI=1S/C8H11N/c1-6-4-3-5-8(9)7(6)2/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
Blockade by ginseng total saponin of methamphetamine-induced hyperactivity and conditioned place preference in mice.
1996 Mar
Effects of ginseng total saponin on morphine-induced hyperactivity and conditioned place preference in mice.
1998 Feb
Determination of the levels of aromatic amines in indoor and outdoor air in Italy.
2001 Apr
An improved synthesis of 5,6-dimethylxanthenone-4-acetic acid (DMXAA).
2002 Oct
Triterpenoids from Glycine max decrease invasiveness and induce caspase-mediated cell death in human SNB19 glioma cells.
2003
Evidence that soyasaponin Bb retards disease progression in a murine model of polycystic kidney disease.
2003 Apr
Natural compounds derived from foods modulate nitric oxide production and oxidative status in epithelial lung cells.
2005 Dec 28
Induction of macroautophagy in human colon cancer cells by soybean B-group triterpenoid saponins.
2005 Jan
Effect of bacosides, alcoholic extract of Bacopa monniera Linn. (brahmi), on experimental amnesia in mice.
2005 Jul
Prediction of genotoxicity of chemical compounds by statistical learning methods.
2005 Jun
Effect of ginseng saponins on enhanced dopaminergic transmission and locomotor hyperactivity induced by nicotine.
2006 Aug
Protective effect of saponins from Panax notoginseng against doxorubicin-induced cardiotoxicity in mice.
2008 Feb
Panax notoginseng saponins attenuate atherosclerosis in rats by regulating the blood lipid profile and an anti-inflammatory action.
2008 Oct
N-(2,3-Dimethyl-phen-yl)-4-hydr-oxy-2-methyl-2H-1,2-benzothia-zine-3-carboxamide 1,1-dioxide.
2009 Feb 28
[Protective effects of AST and ASI on memory impairment and its mechanism in senescent rats treated by GC].
2009 Jan
1-(3-Chloro-benzo-yl)-3-(2,3-dimethyl-phen-yl)thio-urea.
2009 Jan 8
N-(2,3-Dimethyl-phen-yl)-2,4-dimethyl-benzene-sulfonamide.
2010 Apr 2
Bis(2,3-dimethyl-anilinium) dihydrogen-diphosphate.
2010 Feb 6
Ethanol extract and saponin of Platycodon grandiflorum ameliorate scopolamine-induced amnesia in mice.
2010 Jun
Molecular mechanism of endothelial nitric-oxide synthase activation by Platycodon grandiflorum root-derived saponins.
2010 Jun 2
(E)-2,3-Dimethyl-N-(2-nitro-benzyl-idene)aniline.
2010 Jun 26
N-(2,3-Dimethyl-phen-yl)succinimide.
2010 Mar 24
Standardized extracts of Bacopa monniera protect against MPP+- and paraquat-induced toxicity by modulating mitochondrial activities, proteasomal functions, and redox pathways.
2012 Jan
The protective effect of Trillin LPS-induced acute lung injury by the regulations of inflammation and oxidative state.
2016 Jan 5
Global metabolic profiling for the study of Rhizoma Paridis saponins-induced hepatotoxicity in rats.
2017 Jan
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:14:21 GMT 2023
Edited
by admin
on Fri Dec 15 19:14:21 GMT 2023
Record UNII
ZD450ABI9X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,3-XYLIDINE
HSDB  
Systematic Name English
DIMETHYLANILINE, 2,3-
Systematic Name English
BENZENAMINE, 2,3-DIMETHYL-
Systematic Name English
XYLIDINE 2,3-DIMETHYLBENZENAMINE
MI  
Systematic Name English
MEFENAMIC ACID IMPURITY A [EP IMPURITY]
Common Name English
1-AMINO-2,3-DIMETHYLBENZENE
Systematic Name English
2,3-XYLIDINE [HSDB]
Common Name English
2,3-DIMETHYLANILINE [USP-RS]
Common Name English
2,3-DIMETHYLANILINE
USP-RS  
Systematic Name English
2,3-DIMETHYLBENZENAMINE
Systematic Name English
XYLIDINE 2,3-DIMETHYLBENZENAMINE [MI]
Common Name English
Code System Code Type Description
PUBCHEM
6893
Created by admin on Fri Dec 15 19:14:21 GMT 2023 , Edited by admin on Fri Dec 15 19:14:21 GMT 2023
PRIMARY
MERCK INDEX
m11552
Created by admin on Fri Dec 15 19:14:21 GMT 2023 , Edited by admin on Fri Dec 15 19:14:21 GMT 2023
PRIMARY Merck Index
FDA UNII
ZD450ABI9X
Created by admin on Fri Dec 15 19:14:21 GMT 2023 , Edited by admin on Fri Dec 15 19:14:21 GMT 2023
PRIMARY
HSDB
2091
Created by admin on Fri Dec 15 19:14:21 GMT 2023 , Edited by admin on Fri Dec 15 19:14:21 GMT 2023
PRIMARY
CAS
87-59-2
Created by admin on Fri Dec 15 19:14:21 GMT 2023 , Edited by admin on Fri Dec 15 19:14:21 GMT 2023
PRIMARY
ECHA (EC/EINECS)
201-755-0
Created by admin on Fri Dec 15 19:14:21 GMT 2023 , Edited by admin on Fri Dec 15 19:14:21 GMT 2023
PRIMARY
RS_ITEM_NUM
1211254
Created by admin on Fri Dec 15 19:14:21 GMT 2023 , Edited by admin on Fri Dec 15 19:14:21 GMT 2023
PRIMARY
WIKIPEDIA
2,3-Xylidine
Created by admin on Fri Dec 15 19:14:21 GMT 2023 , Edited by admin on Fri Dec 15 19:14:21 GMT 2023
PRIMARY
EPA CompTox
DTXSID3026304
Created by admin on Fri Dec 15 19:14:21 GMT 2023 , Edited by admin on Fri Dec 15 19:14:21 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP