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Details

Stereochemistry ACHIRAL
Molecular Formula C12H10S
Molecular Weight 186.273
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIPHENYL SULFIDE

SMILES

S(C1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=LTYMSROWYAPPGB-UHFFFAOYSA-N
InChI=1S/C12H10S/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10H

HIDE SMILES / InChI

Molecular Formula C12H10S
Molecular Weight 186.273
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Design and synthesis of isonucleosides constructed on a 2-oxa-6-thiabicyclo[3.2.0]heptane scaffold.
2010-06-18
Donor-acceptor-donor fluorene derivatives for two-photon fluorescence lysosomal imaging.
2010-06-18
Carbon nanotube-doped polymer optical fiber.
2009-10-15
Process equipped with a sloped UV lamp for the fabrication of gradient-refractive-index lenses.
2009-05-01
Triplet excited states of some thiophene and triazole substituted platinum(II) acetylide chromophores.
2009-04-09
(3R,6S,7aS)-3-Phenyl-6-(phenyl-sulfan-yl)perhydro-pyrrolo[1,2-c]oxazol-5-one.
2009-04-02
Polystyrene bound oxidovanadium(IV) and dioxidovanadium(V) complexes of histamine derived ligand for the oxidation of methyl phenyl sulfide, diphenyl sulfide and benzoin.
2009-03-28
Development of a novel virtual screening cascade protocol to identify potential trypanothione reductase inhibitors.
2009-03-26
Stereoselective synthesis of a C-linked neuraminic acid disaccharide: potential building block for the synthesis of C-analogues of polysialic acids.
2008-12-05
1-(2,4-Dinitro-phenyl)-3-(4-methyl-phenyl)-4-phenyl-sulfanyl-1H-pyrazole.
2008-10-11
Fabrication of Carbon nanotube poly-methyl-methacrylate composites for nonlinear photonic devices.
2008-07-21
Desulfurization of various organic sulfur compounds and the mixture of DBT + 4,6-DMDBT by Mycobacterium sp. ZD-19.
2008-06
Synthesis and in vivo evaluation of halogenated N,N-dimethyl-2-(2'-amino-4'-hydroxymethylphenylthio)benzylamine derivatives as PET serotonin transporter ligands.
2008-01-24
Electrochemical surface derivatization of glassy carbon by the reduction of triaryl- and alkyldiphenylsulfonium salts.
2008-01-01
Pd/C-catalyzed chemoselective hydrogenation in the presence of diphenylsulfide.
2006-07-20
Photosensitized oxidation of sulfides: discriminating between the singlet-oxygen mechanism and electron transfer involving superoxide anion or molecular oxygen.
2006-06-14
Synthesis and in vitro evaluation of novel derivatives of diphenylsulfide as serotonin transporter ligands.
2006-03-01
Photosensitized oxygenation of sulfides within an amphiphilic dendrimer containing a benzophenone core.
2005-05-12
A facile one-pot benzylation of sodium enolates using trifluoromethanesulfonic anhydride and diphenyl sulfoxide.
2005-05
Determination of the sulphoxides and sulphones of three simple sulphides in rat urine: effects of phenobarbitone, beta-naphthoflavone and methimazole.
2005-01
PET and SPECT exploration of central monoaminergic transporters for the development of new drugs and treatments in brain disorders.
2005
Involvement of cytochrome P450 and the flavin-containing monooxygenase(s) in the sulphoxidation of simple sulphides in human liver microsomes.
2003-06-06
A study of volatile organic sulfur emissions causing urban odors.
2003-04
Conjugated methyl sulfide and phenyl sulfide derivatives of oxidosqualene as inhibitors of oxidosqualene and squalene-hopene cyclases.
2003-03
Molecular modeling of potential new and selective PET radiotracers for the serotonin transporter. Positron Emission Tomography.
2003-01-30
Pharmacological characterization of N,N-dimethyl-2-(2-amino-4-methylphenyl thio)benzylamine as a ligand of the serotonin transporter with high affinity and selectivity.
2003-01
New PET imaging agent for the serotonin transporter: [(18)F]ACF (2-[(2-amino-4-chloro-5-fluorophenyl)thio]-N,N-dimethyl-benzenmethanamine).
2002-10-10
Substituted diphenyl sulfides as selective serotonin transporter ligands: synthesis and in vitro evaluation.
2002-03-14
HPLC analysis of 4-chlorophenyl methyl sulphide and diphenyl sulphide and their corresponding sulphoxides and sulphones in rat liver microsomes.
2002-01-01
Hydroperoxo--copper(II) complex stabilized by N(S)s-type ligand having a phenyl thioether.
2001-08-08
[Substitution of diphenyl sulfurine to trinuclear clusters and infrared spectra characterization].
2001-08
Screening of organosulfur compounds as inhibitors of human CYP2A6.
2001-07
Use of aromatic radical-anions in the absence of THF. Tandem formation and cyclization of benzyllithiums derived from the attack of homo- and bishomoallyllithiums on alpha-methylstyrenes: two-pot synthesis of cuparene.
2001-04-18
Evidence for intermolecular interaction between sulfonium and sulfide sulfur atoms and its application to synthesis of cyclic bis(disulfide) dimer.
2001-03-23
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:57:44 GMT 2025
Edited
by admin
on Mon Mar 31 18:57:44 GMT 2025
Record UNII
B5P3Y93MNR
Record Status Validated (UNII)
Record Version
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Name Type Language
DIPHENYL SULFIDE
MI  
Systematic Name English
NSC-4568
Preferred Name English
DIPHENYL SULPHIDE
Systematic Name English
DIPHENYLMERCAPTAN
Common Name English
DIPHENYL THIOETHER
Systematic Name English
DIPHENYL SULFIDE [MI]
Common Name English
PHENYLSULFIDE
Systematic Name English
1,1'-THIOBISBENZENE
Systematic Name English
PHENYL SULFIDE
Systematic Name English
Code System Code Type Description
CHEBI
38959
Created by admin on Mon Mar 31 18:57:44 GMT 2025 , Edited by admin on Mon Mar 31 18:57:44 GMT 2025
PRIMARY
MERCK INDEX
m4641
Created by admin on Mon Mar 31 18:57:44 GMT 2025 , Edited by admin on Mon Mar 31 18:57:44 GMT 2025
PRIMARY Merck Index
PUBCHEM
8766
Created by admin on Mon Mar 31 18:57:44 GMT 2025 , Edited by admin on Mon Mar 31 18:57:44 GMT 2025
PRIMARY
CAS
139-66-2
Created by admin on Mon Mar 31 18:57:44 GMT 2025 , Edited by admin on Mon Mar 31 18:57:44 GMT 2025
PRIMARY
EPA CompTox
DTXSID8044383
Created by admin on Mon Mar 31 18:57:44 GMT 2025 , Edited by admin on Mon Mar 31 18:57:44 GMT 2025
PRIMARY
MESH
C444009
Created by admin on Mon Mar 31 18:57:44 GMT 2025 , Edited by admin on Mon Mar 31 18:57:44 GMT 2025
PRIMARY
ECHA (EC/EINECS)
205-371-4
Created by admin on Mon Mar 31 18:57:44 GMT 2025 , Edited by admin on Mon Mar 31 18:57:44 GMT 2025
PRIMARY
FDA UNII
B5P3Y93MNR
Created by admin on Mon Mar 31 18:57:44 GMT 2025 , Edited by admin on Mon Mar 31 18:57:44 GMT 2025
PRIMARY
NSC
4568
Created by admin on Mon Mar 31 18:57:44 GMT 2025 , Edited by admin on Mon Mar 31 18:57:44 GMT 2025
PRIMARY