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Details

Stereochemistry ACHIRAL
Molecular Formula C10H9N
Molecular Weight 143.1852
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-METHYLQUINOLINE

SMILES

CC1=CN=C2C=CC=CC2=C1

InChI

InChIKey=DTBDAFLSBDGPEA-UHFFFAOYSA-N
InChI=1S/C10H9N/c1-8-6-9-4-2-3-5-10(9)11-7-8/h2-7H,1H3

HIDE SMILES / InChI

Molecular Formula C10H9N
Molecular Weight 143.1852
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Bis(di-2-pyridyl-methane-diol-κN,O,N')nickel(II) dibenzoate.
2010-09-18
Dibenzoatobis[3-(pyrrol-1-ylmeth-yl)pyridine]-zinc(II).
2010-07-21
Tetra-μ-benzoato-bis-{[4-(pyrrolidin-1-yl)pyridine]zinc(II)}.
2009-12-12
Tetra-μ-benzoato-bis-{[trans-1-(2-pyrid-yl)-2-(4-pyrid-yl)ethyl-ene]zinc(II)}.
2009-11-04
catena-Poly[[bis-(2-hydr-oxy-2-phenyl-acetato-κO,O)zinc(II)]-μ-1,2-di-4-pyridylethane-κN:N'].
2009-08-08
A neutral cubane with a Zn(4)O(4) core: tetra-benzoato-tetra-kis(μ(3)-hydroxydi-2-pyridylmethano-lato)tetra-zinc(II)-acetone-methanol (1/2/1).
2009-05-20
Tetra-μ-benzoato-bis-[(3-methyl-quinoline)copper(II)](Cu-Cu).
2008-08-09
Predictive three-dimensional quantitative structure-activity relationship of cytochrome P450 1A2 inhibitors.
2005-06-02
Replacement of active-site residues of quinoline 2-oxidoreductase involved in substrate recognition and specificity.
2005-04
Quinoline 2-oxidoreductase and 2-oxo-1,2-dihydroquinoline 5,6-dioxygenase from Comamonas testosteroni 63. The first two enzymes in quinoline and 3-methylquinoline degradation.
1995-09-01
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:15:13 GMT 2025
Edited
by admin
on Mon Mar 31 19:15:13 GMT 2025
Record UNII
1YC9RBW2G0
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-109149
Preferred Name English
3-METHYLQUINOLINE
Systematic Name English
QUINOLINE, 3-METHYL-
Systematic Name English
METHYLQUINOLINE, 3-
Systematic Name English
Code System Code Type Description
PUBCHEM
11926
Created by admin on Mon Mar 31 19:15:13 GMT 2025 , Edited by admin on Mon Mar 31 19:15:13 GMT 2025
PRIMARY
CHEBI
20140
Created by admin on Mon Mar 31 19:15:13 GMT 2025 , Edited by admin on Mon Mar 31 19:15:13 GMT 2025
PRIMARY
ECHA (EC/EINECS)
210-315-7
Created by admin on Mon Mar 31 19:15:13 GMT 2025 , Edited by admin on Mon Mar 31 19:15:13 GMT 2025
PRIMARY
CAS
612-58-8
Created by admin on Mon Mar 31 19:15:13 GMT 2025 , Edited by admin on Mon Mar 31 19:15:13 GMT 2025
PRIMARY
NSC
109149
Created by admin on Mon Mar 31 19:15:13 GMT 2025 , Edited by admin on Mon Mar 31 19:15:13 GMT 2025
PRIMARY
FDA UNII
1YC9RBW2G0
Created by admin on Mon Mar 31 19:15:13 GMT 2025 , Edited by admin on Mon Mar 31 19:15:13 GMT 2025
PRIMARY
EPA CompTox
DTXSID60210108
Created by admin on Mon Mar 31 19:15:13 GMT 2025 , Edited by admin on Mon Mar 31 19:15:13 GMT 2025
PRIMARY