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

Details

Stereochemistry ACHIRAL
Molecular Formula C14H12
Molecular Weight 180.2451
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 9,10-DIHYDROPHENANTHRENE

SMILES

C1CC2=CC=CC=C2C3=CC=CC=C13

InChI

InChIKey=XXPBFNVKTVJZKF-UHFFFAOYSA-N
InChI=1S/C14H12/c1-3-7-13-11(5-1)9-10-12-6-2-4-8-14(12)13/h1-8H,9-10H2

HIDE SMILES / InChI

Molecular Formula C14H12
Molecular Weight 180.2451
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Antioxidant biomarkers from Vanda coerulea stems reduce irradiated HaCaT PGE-2 production as a result of COX-2 inhibition.
2010-10-28
10-(2-Eth-oxy-1,3-thia-zol-5-yl)-10-hy-droxy-phenanthren-9(10H)-one.
2010-08-11
Chemical constituents of Asparagus.
2010-07
10-Hy-droxy-10-(1,3-thia-zol-2-ylmeth-yl)phenanthren-9(10H)-one.
2010-06-16
Manganese catalysts for C-H activation: an experimental/theoretical study identifies the stereoelectronic factor that controls the switch between hydroxylation and desaturation pathways.
2010-06-09
Nickel-catalyzed [2+2+2] cycloaddition of arynes and an unactivated alkene: synthesis of 9,10-dihydrophenanthrene derivatives.
2009-07-28
Novel and rapid palladium-assisted 6pi electrocyclic reaction affording 9,10-dihydrophenanthrene and its analogues.
2008-11-06
Rotationally resolved electronic spectra of 9,10-dihydrophenanthrene. A "floppy" molecule in the gas phase.
2007-06-14
9, 10-Dihydrophenanthrene derivatives from Pholidota yunnanensis and scavenging activity on DPPH free radical.
2007-03
Carbocyclization of aromatic iodides, bicyclic alkenes, and benzynes involving a palladium-catalyzed C-H bond activation as a key step.
2006-11-23
Photophysical and photochemical processes of 9,10-dihydro-9-silaphenanthrene derivatives: photochemical formation and electronic structure of 9-silaphenanthrenes.
2006-03-23
Competitive 1,2- and 1,5-hydrogen shifts following 2-vinylbiphenyl photocyclization.
2005-12-09
Ring-closing photoisomerization of some 2,6-diarylstyrenes.
2005-07-19
Palladium-catalyzed [2 + 2 + 2] cocyclotrimerization of benzynes with bicyclic alkenes: an efficient route to anellated 9,10-dihydrophenanthrene derivatives and polyaromatic compounds.
2004-11-26
Temperature dependence of the infinite dilution activity coefficient and Henry's law constant of polycyclic aromatic hydrocarbons in water.
2004-08
Thermal decomposition of O-benzyl ketoximes; role of reverse radical disproportionation.
2004-02-07
Electrochiroptical response of 2,2'-(2,2-diarylethenyl)binaphthyl-type electron donors that undergo reversible C-C bond formation/breaking upon two-electron transfer.
2003-08-22
De novo design, synthesis, and evaluation of novel nonsteroidal phenanthrene ligands for the estrogen receptor.
2003-04-10
Symmetry-enforced conformational control of photochemical reactivity in 2-vinyl-1,3-terphenyl.
2002-11-20
Circular dichroism of 9,10-dihydrophenanthrene derivatives reveals both the absolute configuration and conformation: a novel approach to Mislow's helicity rule.
2002-09-16
Phenanthrene derivatives from the orchid Coelogyne cristata.
2001-10
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:50:22 GMT 2025
Edited
by admin
on Mon Mar 31 19:50:22 GMT 2025
Record UNII
BRM9TU2F34
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-60018
Preferred Name English
9,10-DIHYDROPHENANTHRENE
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
212-278-2
Created by admin on Mon Mar 31 19:50:22 GMT 2025 , Edited by admin on Mon Mar 31 19:50:22 GMT 2025
PRIMARY
EPA CompTox
DTXSID20228264
Created by admin on Mon Mar 31 19:50:22 GMT 2025 , Edited by admin on Mon Mar 31 19:50:22 GMT 2025
PRIMARY
PUBCHEM
13058
Created by admin on Mon Mar 31 19:50:22 GMT 2025 , Edited by admin on Mon Mar 31 19:50:22 GMT 2025
PRIMARY
NSC
60018
Created by admin on Mon Mar 31 19:50:22 GMT 2025 , Edited by admin on Mon Mar 31 19:50:22 GMT 2025
PRIMARY
FDA UNII
BRM9TU2F34
Created by admin on Mon Mar 31 19:50:22 GMT 2025 , Edited by admin on Mon Mar 31 19:50:22 GMT 2025
PRIMARY
CAS
776-35-2
Created by admin on Mon Mar 31 19:50:22 GMT 2025 , Edited by admin on Mon Mar 31 19:50:22 GMT 2025
PRIMARY