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358916

Sigma-Aldrich

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
Beilstein:
105686
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

crystals

mp

48-50 °C (lit.)

functional group

thioether

SMILES string

S=C1SC=CS1

InChI

1S/C3H2S3/c4-3-5-1-2-6-3/h1-2H

InChI key

WYKJWNVWJOKVQP-UHFFFAOYSA-N

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General description

Vinylene trithiocarbonate has been investigated as electrolyte additive for use in lithium ion batteries.

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.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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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)
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
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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