358916
Vinylene trithiocarbonate
98%
Synonym(s):
1,3-Dithiole-2-thione
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About This Item
Empirical Formula (Hill Notation):
C3H2S3
CAS Number:
Molecular Weight:
134.24
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
213-215-1
Beilstein/REAXYS Number:
105686
MDL number:
Product Name
Vinylene trithiocarbonate, 98%
InChI key
WYKJWNVWJOKVQP-UHFFFAOYSA-N
InChI
1S/C3H2S3/c4-3-5-1-2-6-3/h1-2H
SMILES string
S=C1SC=CS1
assay
98%
form
crystals
mp
48-50 °C (lit.)
functional group
thioether
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Application
Vinylene trithiocarbonate may be used in the synthesis of series of symmetrical 1,3-dithiole-2-thiones and -ones. It is suitable for use as substrate to investigate the omega class glutathione S-transferase enzymatic activity.
General description
Vinylene trithiocarbonate has been investigated as electrolyte additive for use in lithium ion batteries.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Javier Girardini et al.
European journal of biochemistry, 269(22), 5512-5521 (2002-11-09)
Glutathione S-transferases (EC 2.5.1.18) (GSTs), are a family of multifunctional enzymes present in all living organisms whose main function is the detoxification of electrophilic compounds. GSTs are considered the most prominent detoxifying class II enzymes in helminths. We describe here
A combined substituent and supramolecular approach for improving the electron donor properties of 1, 3-dithiole-2-thione derivatives.
Khan T, et al.
Journal of Materials Chemistry, 13(10), 2490-2498 (2003)
Vinylene carbonate and vinylene trithiocarbonate as electrolyte additives for lithium ion battery.
Chang C-C, et al.
Journal of Power Sources, 196(22), 9605-9611 (2011)
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