N-Methyl-2-thiazolidinethione

Last updated
N-Methyl-2-thiazolidinethione
N-Methyl-2-thiazolidinethione.svg
Names
Preferred IUPAC name
3-Methyl-1,3-thiazolidine-2-thione
Other names
MTT, MTT 80, N-Methyl-2-thiazolidinethione
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.016.014 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 217-614-1
PubChem CID
UNII
  • InChI=1S/C4H7NS2/c1-5-2-3-7-4(5)6/h2-3H2,1H3
    Key: RGTLAJIDOSPEDH-UHFFFAOYSA-N
  • CN1CCSC1=S
Properties
C4H7NS2
Molar mass 133.23 g·mol−1
AppearanceWhite solid
Melting point 68–69 °C (154–156 °F; 341–342 K)
Hazards
GHS pictograms GHS-pictogram-exclam.svg
GHS Signal word Warning
H302
P264, P270, P301+312, P330, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

N-Methyl-2-thiazolidinethione is the organosulfur compound with the formula C2H4S(NCH3)CS. It is classified as a heterocycle called a thiazolidine. It is a colorless or off-white solid. It has gained attention as a proposed low toxicity replacement for ethylenethioureas, which are used as accelerators for the vulcanization of chloroprene rubbers. [1] The compound is prepared by reaction of N-methylethanolamine and carbon disulfide.

See also

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Benzothiazole Chemical compound

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7
H
5
NS
. It is colorless, slightly viscous liquid. Although the parent compound, benzothiazole is not widely used, many of its derivatives are found in commercial products or in nature. Firefly luciferin can be considered a derivative of benzothiazole.

Thiazolidine is a heterocyclic organic compound with the formula (CH2)3(NH)S. It is a 5-membered saturated ring with a thioether group and an amine group in the 1 and 3 positions. It is a sulfur analog of oxazolidine. Thiazolidine is a colorless liquid.

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2-Mercaptobenzothiazole is an organosulfur compound with the formula C
6
H
4
(NH)SC=S
. It is used in the sulfur vulcanization of rubber.

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References

  1. Rüdiger Schubart (2000). "Dithiocarbamic Acid and Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a09_001.