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
SMILES
CC1=CC(N)=CC(C)=C1
InChI
InChIKey=MKARNSWMMBGSHX-UHFFFAOYSA-N
InChI=1S/C8H11N/c1-6-3-7(2)5-8(9)4-6/h3-5H,9H2,1-2H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| N-(3,5-Dimethyl-phen-yl)succinamic acid. | 2010-12-24 |
|
| 1-(3,5-Dimethyl-phen-yl)-4,5-dimethyl-2-phenyl-1H-imidazole hemihydrate. | 2010-10-09 |
|
| Monocyclic aromatic amines as potential human carcinogens: old is new again. | 2010-01 |
|
| Tetra-kis(3,5-xylidinium) dihydrogen cyclo-hexa-phosphate dihydrate. | 2009-12-24 |
|
| N-(3,5-Dimethyl-phen-yl)-4-methyl-benzene-sulfonamide. | 2009-12-16 |
|
| N-(3,5-Dimethyl-phen-yl)benzene-sulfonamide. | 2009-11-28 |
|
| Separation and analysis of dimethylaniline isomers by supercritical fluid chromatography--electrospray ionization tandem mass spectrometry. | 2009-10-09 |
|
| Ethyl 3-[(3,5-dimethyl-phen-yl)amino-carbon-yl]propanoate. | 2009-07-29 |
|
| Identification of adducts formed by reaction of N-acetoxy-3,5-dimethylaniline with DNA. | 2007-11 |
|
| Arylamine N-acetyltransferases: characterization of the substrate specificities and molecular interactions of environmental arylamines with human NAT1 and NAT2. | 2007-09 |
|
| Pi-Pi complexation of bupivacaine and analogues with aromatic receptors: implications for overdose remediation. | 2007 |
|
| Identification and characterization of functional rat arylamine N-acetyltransferase 3: comparisons with rat arylamine N-acetyltransferases 1 and 2. | 2006-10 |
|
| DNA adduct formation by 2,6-dimethyl-, 3,5-dimethyl-, and 3-ethylaniline in vivo in mice. | 2006-08 |
|
| Fabrication of a metal nanoparticles and polymer nanofibers composite material by an in situ chemical synthetic route. | 2005-08-16 |
|
| Alkylaniline-hemoglobin adducts and risk of non-smoking-related bladder cancer. | 2004-10-06 |
|
| 2,4-disubstituted pyrimidines: a novel class of KDR kinase inhibitors. | 2003-05-19 |
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| Code System | Code | Type | Description | ||
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C514328
Created by
admin on Mon Mar 31 19:18:52 GMT 2025 , Edited by admin on Mon Mar 31 19:18:52 GMT 2025
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PRIMARY | |||
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3,5-Xylidine
Created by
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203-607-0
Created by
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2096
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7949
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26880
Created by
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108-69-0
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m11552
Created by
admin on Mon Mar 31 19:18:52 GMT 2025 , Edited by admin on Mon Mar 31 19:18:52 GMT 2025
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DTXSID8026309
Created by
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1418BR6T2H
Created by
admin on Mon Mar 31 19:18:52 GMT 2025 , Edited by admin on Mon Mar 31 19:18:52 GMT 2025
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SUBSTANCE RECORD
