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33820

Sigma-Aldrich

Dibenzyl sulfide

≥95.0% (HPLC)

Sinônimo(s):

Benzyl sulfide

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About This Item

Fórmula linear:
(C6H5CH2)2S
Número CAS:
538-74-9
Peso molecular:
214.33
Beilstein:
1911157
Número CE:
208-703-6
Número MDL:
MFCD00004784
Código UNSPSC:
12352100
ID de substância PubChem:
57648912
NACRES:
NA.22

Nível de qualidade

100

Ensaio

≥95.0% (HPLC)

Formulário

solid

pf

44-47 °C (lit.)

grupo funcional

phenyl
thioether

cadeia de caracteres SMILES

C(SCc1ccccc1)c2ccccc2

InChI

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

chave InChI

LUFPJJNWMYZRQE-UHFFFAOYSA-N

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Descrição geral

Sulfur K-edge XANES spectra of dibenzyl sulfide has been measured. Adsorption modes of dibenzyl disulphide on bare and iron-coated silver in 0.5M HCl was studied by surface-enhanced Raman scattering (SERS) spectroscopy. Dibenzyl sulfide undergoes oxidation to dibenzyl sulfoxide by SiO2-HNO3/KBr.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

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Vered Heleg-Shabtai et al.
Advances in experimental medicine and biology, 733, 53-61 (2011-11-22)
The improvements in Raman instrumentation have led to the development of -portable, simple to operate, Raman instruments that can be used for on-site analysis of substances relevant for homeland security purposes such as chemical and biological warfare and explosives materials.Raman
Eun Kyoung Ryu et al.
Bioorganic & medicinal chemistry, 12(5), 859-864 (2004-02-26)
Benzyl 4-halobenzyl and ally benzyl disulfide were synthesized as diallyl disulfide analogues and their tumor growth inhibitory effects on the cancer cells (SNU C5 and MCF-7) were comparable to that of diallyl disulfide, indicating that the disulfide functional group was
Robert Beck et al.
Dalton transactions (Cambridge, England : 2003), (37)(37), 4981-4983 (2008-09-20)
C-H activation through the coordination of a benzyl sulfide anchoring group with a C-S bond cleavage at a Co(v) center constitutes a regiospecific access to four- and five-membered metallacycles under mild conditions.
Chemo and homoselective catalytic oxidation of sulfides to sulfoxides with supported nitric acid on silica gel and poly vinyl pyrrolidone (PVP) catalyzed by KBr and/or NaBr.
Zolfigol MA, et al.
Catalysis Communications, 9(8), 1739-1744 (2008)
B Lei et al.
Journal of bacteriology, 178(19), 5699-5705 (1996-10-01)
The oxidation of dibenzothiophene to dibenzothiophene sulfone has been linked to the enzyme encoded by the sox/dszC gene from Rhodococcus sp. strain IGTS8 (S. A. Denome, C. Oldfield, L. J. Nash, and K. D. Young, J. Bacteriol. 176:6707-6717, 1994; C.
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