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Merck
CN

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:
Assay:
98%
Form:
crystals
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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

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

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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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)
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



Global Trade Item Number

SKUGTIN
358916-5G04061832425153
358916-1G04061825895208