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Details

Stereochemistry ACHIRAL
Molecular Formula C15H12
Molecular Weight 192.2558
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-METHYLANTHRACENE

SMILES

CC1=CC=C2C=C3C=CC=CC3=CC2=C1

InChI

InChIKey=GYMFBYTZOGMSQJ-UHFFFAOYSA-N
InChI=1S/C15H12/c1-11-6-7-14-9-12-4-2-3-5-13(12)10-15(14)8-11/h2-10H,1H3

HIDE SMILES / InChI

Molecular Formula C15H12
Molecular Weight 192.2558
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Line broadening in electronic spectra of anthracene derivatives inside superfluid helium nanodroplets.
2010-09-21
Tumor promoting properties of a cigarette smoke prevalent polycyclic aromatic hydrocarbon as indicated by the inhibition of gap junctional intercellular communication via phosphatidylcholine-specific phospholipase C.
2008-04
Degradation of polycyclic aromatic hydrocarbons by Rigidoporus lignosus and its laccase in the presence of redox mediators.
2008-04
Comprehensive photoelectron spectroscopic study of anionic clusters of anthracene and its alkyl derivatives: electronic structures bridging molecules to bulk.
2007-12-21
Concentrations of methylated naphthalenes, anthracenes, and phenanthrenes occurring in Czech river sediments and their effects on toxic events associated with carcinogenesis in rat liver cell lines.
2007-11
Cigarette smoke components inhibited intercellular communication and differentiation in human pancreatic ductal epithelial cells.
2007-05-01
Effects of derivatization on solar-induced decomposition of polycyclic aromatic hydrocarbons in aqueous media.
2007-02-15
Dual fluorescence of 2-methoxyanthracene derivatives.
2007-02-15
Structure-activity relationships for flow cytometric data of smaller polycyclic aromatic hydrocarbons.
2006-12
Manganese-lignin peroxidase hybrid from Bjerkandera adusta oxidizes polycyclic aromatic hydrocarbons more actively in the absence of manganese.
2003-11
Efficient preparation of monoadducts of [60] fullerene and anthracenes by solution chemistry and their thermolytic decomposition in the solid state.
2001-08-03
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:48:42 GMT 2025
Edited
by admin
on Mon Mar 31 19:48:42 GMT 2025
Record UNII
6C868JOV4A
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-87376
Preferred Name English
2-METHYLANTHRACENE
Systematic Name English
Code System Code Type Description
CAS
613-12-7
Created by admin on Mon Mar 31 19:48:42 GMT 2025 , Edited by admin on Mon Mar 31 19:48:42 GMT 2025
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EPA CompTox
DTXSID8060616
Created by admin on Mon Mar 31 19:48:42 GMT 2025 , Edited by admin on Mon Mar 31 19:48:42 GMT 2025
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FDA UNII
6C868JOV4A
Created by admin on Mon Mar 31 19:48:42 GMT 2025 , Edited by admin on Mon Mar 31 19:48:42 GMT 2025
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ECHA (EC/EINECS)
210-329-3
Created by admin on Mon Mar 31 19:48:42 GMT 2025 , Edited by admin on Mon Mar 31 19:48:42 GMT 2025
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NSC
87376
Created by admin on Mon Mar 31 19:48:42 GMT 2025 , Edited by admin on Mon Mar 31 19:48:42 GMT 2025
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MESH
C051247
Created by admin on Mon Mar 31 19:48:42 GMT 2025 , Edited by admin on Mon Mar 31 19:48:42 GMT 2025
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PUBCHEM
11936
Created by admin on Mon Mar 31 19:48:42 GMT 2025 , Edited by admin on Mon Mar 31 19:48:42 GMT 2025
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