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Details

Stereochemistry ACHIRAL
Molecular Formula C14H14S
Molecular Weight 214.326
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BENZYL SULFIDE

SMILES

C(SCC1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=LUFPJJNWMYZRQE-UHFFFAOYSA-N
InChI=1S/C14H14S/c1-3-7-13(8-4-1)11-15-12-14-9-5-2-6-10-14/h1-10H,11-12H2

HIDE SMILES / InChI

Molecular Formula C14H14S
Molecular Weight 214.326
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Dibenzyl sulfoxide.
2010-12-18
Functional groups and sulfur K-edge XANES spectra: divalent sulfur and disulfides.
2010-09-09
A combined theoretical and experimental investigation on the enantioselective oxidation of aryl benzyl sulfides in the presence of a chiral titanium catalyst.
2009-12-14
Petiveria alliacea extracts uses multiple mechanisms to inhibit growth of human and mouse tumoral cells.
2008-11-18
Four- and five-membered cobaltacycles by regioselective cyclometallation of benzyl sulfide derivatives via Co(v) intermediates.
2008-10-07
Characterization of diverse Acinetobacter isolates for utilization of multiple aromatic compounds.
2008-05
Cis/trans isomers of PtX(2)L(2) (X = halogen, L = neutral ligand); the crystal structures of two polymorphs of cis-dichlorobis(dibenzyl sulfido-kappaS)platinum(II) in the temperature range 100-295 K.
2008-04
C-H bond oxidation initiated pummerer- and Knoevenagel-type reactions of benzyl sulfide and 1,3-dicarbonyl compounds.
2008-03-06
Singlet oxygen promoted carbon-heteroatom bond cleavage in dibenzyl sulfides and tertiary dibenzylamines. Structural effects and the role of exciplexes.
2007-12-07
Selectivity among organic sulfur compounds in one- and two-liquid-phase cultures of Rhodococcus sp. strain JVH1.
2007-08
On the cytotoxicity and status of oxidative stress of two novel synthesized tri-aza macrocyclic diamides as studied in the V79 cell lines.
2007-05-15
Studies on the mechanism of action of prekinamycin, a member of the diazoparaquinone family of natural products: evidence for both sp2 radical and orthoquinonemethide intermediates.
2006-09-27
Carbosilane dendrimers bearing globotriaoses: syntheses of globotrioasyl derivative and introduction into carbosilane dendrimers.
2006-08
Antibacterial and antifungal activity of sulfur-containing compounds from Petiveria alliacea L.
2006-03-08
Bacterial biodegradation of aliphatic sulfides under aerobic carbon- or sulfur-limited growth conditions.
2005
Dendrimer interior functional group conversion and dendrimer metamorphosis--new approaches to the synthesis of oligo(dibenzyl sulfone) and oligo(phenylenevinylene) dendrimers.
2004-10-13
New antibacterial agents derived from the DNA gyrase inhibitor cyclothialidine.
2004-03-11
Synthesis of radioiodine labeled dibenzyl disulfide for evaluation of tumor cell uptake.
2004-03-01
New protocol for oxidation in water: micellar oxidation systems composed of novel amphiphilic hydroperoxides.
2004-01-06
Dibenzyl sulfide metabolism by white rot fungi.
2003-02
Substitution reactions on cyclometalated Pt(IV) complexes. Associative tuning by fluoro ligands and fluorinated substituents.
2002-04-08
Disassembly of microtubules and inhibition of neurite outgrowth, neuroblastoma cell proliferation, and MAP kinase tyrosine dephosphorylation by dibenzyl trisulphide.
2001-08-22
Fungal cleavage of thioether bond found in Yperite.
1997-07-28
Gene overexpression, purification, and identification of a desulfurization enzyme from Rhodococcus sp. strain IGTS8 as a sulfide/sulfoxide monooxygenase.
1996-10
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:47:21 GMT 2025
Edited
by admin
on Mon Mar 31 18:47:21 GMT 2025
Record UNII
Q08048624M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-212544
Preferred Name English
BENZYL SULFIDE
HSDB   MI  
Systematic Name English
BENZYL SULFIDE [MI]
Common Name English
BENZYL SULPHIDE
Systematic Name English
BENZYL SULFIDE [HSDB]
Common Name English
Code System Code Type Description
MESH
C016367
Created by admin on Mon Mar 31 18:47:21 GMT 2025 , Edited by admin on Mon Mar 31 18:47:21 GMT 2025
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NSC
212544
Created by admin on Mon Mar 31 18:47:21 GMT 2025 , Edited by admin on Mon Mar 31 18:47:21 GMT 2025
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CAS
538-74-9
Created by admin on Mon Mar 31 18:47:21 GMT 2025 , Edited by admin on Mon Mar 31 18:47:21 GMT 2025
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FDA UNII
Q08048624M
Created by admin on Mon Mar 31 18:47:21 GMT 2025 , Edited by admin on Mon Mar 31 18:47:21 GMT 2025
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PUBCHEM
10867
Created by admin on Mon Mar 31 18:47:21 GMT 2025 , Edited by admin on Mon Mar 31 18:47:21 GMT 2025
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ECHA (EC/EINECS)
208-703-6
Created by admin on Mon Mar 31 18:47:21 GMT 2025 , Edited by admin on Mon Mar 31 18:47:21 GMT 2025
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HSDB
2794
Created by admin on Mon Mar 31 18:47:21 GMT 2025 , Edited by admin on Mon Mar 31 18:47:21 GMT 2025
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WIKIPEDIA
Dibenzyl sulfide
Created by admin on Mon Mar 31 18:47:21 GMT 2025 , Edited by admin on Mon Mar 31 18:47:21 GMT 2025
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EPA CompTox
DTXSID6024599
Created by admin on Mon Mar 31 18:47:21 GMT 2025 , Edited by admin on Mon Mar 31 18:47:21 GMT 2025
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MERCK INDEX
m2417
Created by admin on Mon Mar 31 18:47:21 GMT 2025 , Edited by admin on Mon Mar 31 18:47:21 GMT 2025
PRIMARY Merck Index