Skip to Content
Merck
CN

440779

Dimethyl 2-thioxo-1,3-dithiole-4,5-dicarboxylate

98%

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Empirical Formula (Hill Notation):
C7H6O4S3
CAS Number:
Molecular Weight:
250.32
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1288368
Assay:
98%
Form:
solid
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

Dimethyl 2-thioxo-1,3-dithiole-4,5-dicarboxylate, 98%

InChI

1S/C7H6O4S3/c1-10-5(8)3-4(6(9)11-2)14-7(12)13-3/h1-2H3

SMILES string

COC(=O)C1=C(SC(=S)S1)C(=O)OC

InChI key

UZKKFHMMXWDIPD-UHFFFAOYSA-N

assay

98%

form

solid

mp

86-90 °C (lit.)

functional group

ester
thioether

Looking for similar products? Visit Product Comparison Guide

General description

Dimethyl 2-thioxo-1,3-dithiole-4,5-dicarboxylate is a sulphur-containing heterocyclic building block. It has been reported to be formed during the reaction of 1,3-dithiolan-2-thiones with dimethyl acetylenedicarboxylate. It is formed as major product during the reaction of ethylene trithiocarbonate with dimethyl acetylenedicarboxylate.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

The dithiole series. Part V. Reactions of 1, 2-dithiole-3-thiones and 1, 3-dithiolan-2-thiones with acetylenic esters and with benzyne.
Easton DBJ, et al.
Journal of the Chemical Society. Perkin Transactions 1, 41-45 (1972)
The pyridazine-tetrathiafulvalene conjugates: synthesis, photophysical, and electrochemical properties.
Zheng N, et al.
Tetrahedron, 68(6), 1782-1789 (2012)
New thiopyran-4-spiro-2'-(1, 3-dithiolane): Formation mechanism and crystal structure.
Li HQ, et al.
CRC Handbook of Thermoelectronics, 22(3), 280-283 (2011)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service