33820
ジベンジルスルフィド
≥95.0% (HPLC)
別名:
硫化ベンジル
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この商品について
化学式:
(C6H5CH2)2S
CAS番号:
分子量:
214.33
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-703-6
Beilstein/REAXYS Number:
1911157
MDL number:
Assay:
≥95.0% (HPLC)
Form:
solid
Quality Level
assay
≥95.0% (HPLC)
form
solid
mp
44-47 °C (lit.)
functional group
phenyl, thioether
SMILES string
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
InChI key
LUFPJJNWMYZRQE-UHFFFAOYSA-N
General description
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.
保管分類
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
I L Genz et al.
Zentralblatt fur Bakteriologie, Parasitenkunde, Infektionskrankheiten und Hygiene. Zweite naturwissenschaftliche Abteilung: Mikrobiologie der Landwirtschaft der Technologie und des Umweltschutzes, 135(4), 308-312 (1980-01-01)
A diffusion cell type which is suitable for investigation of water-insoluble compounds is shown. The chamber consists of two compartments, the so-called bottom-chamber, which contains the solid substance under investigation, and the main chamber, which is above it. In this
N Itoh et al.
FEBS letters, 412(2), 281-284 (1997-07-28)
The degradation of thiodiglycol (I) and benzyl sulfide (II) was attempted using Coriolus versicolor and Tyromyces palustris to investigate the potential ability of basidiomycetes to degrade Yperite (bis(2-chloroethyl) sulfide), a mass-produced and stored chemical warfare agent. I was very rapidly
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