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线性分子式:
C6H5SSC6H5
化学文摘社编号:
分子量:
218.34
PubChem Substance ID:
UNSPSC Code:
12164502
Council of Europe no.:
11757
FEMA Number:
3225
Flavis number:
12.043
EC Number:
212-926-4
MDL number:
Beilstein/REAXYS Number:
639794
InChI key
GUUVPOWQJOLRAS-UHFFFAOYSA-N
InChI
1S/C12H10S2/c1-3-7-11(8-4-1)13-14-12-9-5-2-6-10-12/h1-10H
SMILES string
S(Sc1ccccc1)c2ccccc2
biological source
synthetic
grade
Halal, Kosher
assay
≥98%
mp
58-60 °C (lit.)
application(s)
flavors and fragrances
documentation
see Safety & Documentation for available documents
food allergen
no known allergens
organoleptic
earthy; sulfurous
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Other Notes
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
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J I Rossato et al.
Neurochemical research, 27(4), 297-303 (2002-04-18)
Ebselen (2-phenyl- 1,2-benzisoselenazole-3 (2H)-one) is a seleno-organic compound with antioxidant properties, and anti-inflammatory actions. Recently, ebselen improved the outcome of acute ischemic stroke in humans. In the present study, the potential antioxidant capacity of organochalcogenide compounds diphenyl diselenide (PhSe)2, diphenyl
C W Nogueira et al.
Toxicology, 191(2-3), 169-178 (2003-09-11)
Organochalcogens are important intermediates and useful reagents in organic synthesis, which can increase human exposure risk to these chemicals in the workplace. As well, there are a number of reported cases of acute toxicity following organochalcogen ingestion of vitamins and
E W Srikendari et al.
Redox report : communications in free radical research, 6(3), 191-193 (2001-08-29)
The aim of this study was to determine whether disulfides could serve as protective antioxidants for alpha-tocopherol or vice versa. The chosen reaction system was a co-oxidation of the model compound of alpha-tocopherol, 2,2,5,7,8-pentamethyl-6-chromanol (PMC), and diphenyl disulfide (1) by
Patricia J Lee et al.
Journal of medicinal chemistry, 52(4), 952-963 (2009-02-05)
The importance of fatty acids to the human malaria parasite, Plasmodium falciparum, and differences due to a type I fatty acid synthesis (FAS) pathway in the parasite, make it an attractive drug target. In the present study, we developed and
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