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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
Gene overexpression, purification, and identification of a desulfurization enzyme from Rhodococcus sp. strain IGTS8 as a sulfide/sulfoxide monooxygenase.
1996 Oct
Fungal cleavage of thioether bond found in Yperite.
1997 Jul 28
Disassembly of microtubules and inhibition of neurite outgrowth, neuroblastoma cell proliferation, and MAP kinase tyrosine dephosphorylation by dibenzyl trisulphide.
2001 Aug 22
Substitution reactions on cyclometalated Pt(IV) complexes. Associative tuning by fluoro ligands and fluorinated substituents.
2002 Apr 8
Dibenzyl sulfide metabolism by white rot fungi.
2003 Feb
New protocol for oxidation in water: micellar oxidation systems composed of novel amphiphilic hydroperoxides.
2004 Jan 6
Synthesis of radioiodine labeled dibenzyl disulfide for evaluation of tumor cell uptake.
2004 Mar 1
New antibacterial agents derived from the DNA gyrase inhibitor cyclothialidine.
2004 Mar 11
Dendrimer interior functional group conversion and dendrimer metamorphosis--new approaches to the synthesis of oligo(dibenzyl sulfone) and oligo(phenylenevinylene) dendrimers.
2004 Oct 13
Bacterial biodegradation of aliphatic sulfides under aerobic carbon- or sulfur-limited growth conditions.
2005
Carbosilane dendrimers bearing globotriaoses: syntheses of globotrioasyl derivative and introduction into carbosilane dendrimers.
2006 Aug
Antibacterial and antifungal activity of sulfur-containing compounds from Petiveria alliacea L.
2006 Mar 8
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 Sep 27
Selectivity among organic sulfur compounds in one- and two-liquid-phase cultures of Rhodococcus sp. strain JVH1.
2007 Aug
Singlet oxygen promoted carbon-heteroatom bond cleavage in dibenzyl sulfides and tertiary dibenzylamines. Structural effects and the role of exciplexes.
2007 Dec 7
On the cytotoxicity and status of oxidative stress of two novel synthesized tri-aza macrocyclic diamides as studied in the V79 cell lines.
2007 May 15
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 Apr
C-H bond oxidation initiated pummerer- and Knoevenagel-type reactions of benzyl sulfide and 1,3-dicarbonyl compounds.
2008 Mar 6
Characterization of diverse Acinetobacter isolates for utilization of multiple aromatic compounds.
2008 May
Petiveria alliacea extracts uses multiple mechanisms to inhibit growth of human and mouse tumoral cells.
2008 Nov 18
Four- and five-membered cobaltacycles by regioselective cyclometallation of benzyl sulfide derivatives via Co(v) intermediates.
2008 Oct 7
A combined theoretical and experimental investigation on the enantioselective oxidation of aryl benzyl sulfides in the presence of a chiral titanium catalyst.
2009 Dec 14
Dibenzyl sulfoxide.
2010 Dec 18
Functional groups and sulfur K-edge XANES spectra: divalent sulfur and disulfides.
2010 Sep 9
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:29:47 UTC 2023
Edited
by admin
on Fri Dec 15 17:29:47 UTC 2023
Record UNII
Q08048624M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BENZYL SULFIDE
HSDB   MI  
Systematic Name English
BENZYL SULFIDE [MI]
Common Name English
NSC-212544
Code English
BENZYL SULPHIDE
Systematic Name English
BENZYL SULFIDE [HSDB]
Common Name English
Code System Code Type Description
MESH
C016367
Created by admin on Fri Dec 15 17:29:47 UTC 2023 , Edited by admin on Fri Dec 15 17:29:47 UTC 2023
PRIMARY
NSC
212544
Created by admin on Fri Dec 15 17:29:47 UTC 2023 , Edited by admin on Fri Dec 15 17:29:47 UTC 2023
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CAS
538-74-9
Created by admin on Fri Dec 15 17:29:47 UTC 2023 , Edited by admin on Fri Dec 15 17:29:47 UTC 2023
PRIMARY
FDA UNII
Q08048624M
Created by admin on Fri Dec 15 17:29:47 UTC 2023 , Edited by admin on Fri Dec 15 17:29:47 UTC 2023
PRIMARY
PUBCHEM
10867
Created by admin on Fri Dec 15 17:29:47 UTC 2023 , Edited by admin on Fri Dec 15 17:29:47 UTC 2023
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ECHA (EC/EINECS)
208-703-6
Created by admin on Fri Dec 15 17:29:47 UTC 2023 , Edited by admin on Fri Dec 15 17:29:47 UTC 2023
PRIMARY
HSDB
2794
Created by admin on Fri Dec 15 17:29:47 UTC 2023 , Edited by admin on Fri Dec 15 17:29:47 UTC 2023
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WIKIPEDIA
Dibenzyl sulfide
Created by admin on Fri Dec 15 17:29:47 UTC 2023 , Edited by admin on Fri Dec 15 17:29:47 UTC 2023
PRIMARY
EPA CompTox
DTXSID6024599
Created by admin on Fri Dec 15 17:29:47 UTC 2023 , Edited by admin on Fri Dec 15 17:29:47 UTC 2023
PRIMARY
MERCK INDEX
m2417
Created by admin on Fri Dec 15 17:29:47 UTC 2023 , Edited by admin on Fri Dec 15 17:29:47 UTC 2023
PRIMARY Merck Index