440779
1,3-二硫杂环戊烯-2-硫酮-4,5-二甲酸二甲酯
98%
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关于此项目
经验公式（希尔记法）:
C7H6O4S3
化学文摘社编号:
分子量:
250.32
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1288368
Assay:
98%
Form:
solid
产品名称
1,3-二硫杂环戊烯-2-硫酮-4,5-二甲酸二甲酯, 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
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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.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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)
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