822-38-8

  • Product Name:Ethylene Trithiocarbonate
  • Molecular Formula:C3H4S3
  • Purity:99%
  • Molecular Weight:136.263
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Product Details;

CasNo: 822-38-8

Molecular Formula: C3H4S3

Appearance: Yellow low melting solid

factory and supplier 822-38-8 Ethylene Trithiocarbonate in stock

  • Molecular Formula:C3H4S3
  • Molecular Weight:136.263
  • Appearance/Colour:Yellow low melting solid 
  • Vapor Pressure:0.00135mmHg at 25°C 
  • Melting Point:34-36 °C(lit.) 
  • Refractive Index:1.732 
  • Boiling Point:307 °C at 760 mmHg 
  • Flash Point:139.5 °C 
  • PSA:82.69000 
  • Density:1.47 g/cm3 
  • LogP:1.75130 

ETHYLENE TRITHIOCARBONATE(Cas 822-38-8) Usage

InChI:InChI=1/C3H4S3/c4-3-5-1-2-6-3/h1-2H2

822-38-8 Relevant articles

The Reactions of the 1,2-Ethanediylbis(trithiocarbonic acid) Dianion with Several Electrophilic Reagents

Tanimoto, Shigeo,Oida, Tatsuo,Kokubo, Toshio,Okano, Masaya

, p. 339 - 340 (1982)

It has been found that the reaction of t...

-

Braun,Kiessel

, p. 631,636,638,641 (1965)

-

A convenient one-pot method for the synthesis of symmetrical dialkyl trithiocarbonates using NH4OAc under mild neutral conditions

Arzehgar, Zeinab,Ahmadi, Hosna

, p. 303 - 306 (2018/11/01)

A facial, new, one-pot method for the pr...

Reaction of three cyclic thioester ligands with triiron dodecacarbonyl and possible reaction mechanisms

Xiao, Zhiyin,Wang, Yongli,Chen, Xueyuan,Long, Jiao,Wei, Zhenhong

, p. 1595 - 1601 (2017/11/03)

Abstract : Three cyclic thioesters of th...

Atom economical synthesis of di- and trithiocarbonates by the lithium: Tert -butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes

Diebler,Spannenberg,Werner

supporting information, p. 7480 - 7489 (2016/08/16)

Alkali metal alkoxides were studied as c...

Superbasic system CsOH/DMSO as a reagent for a fast one-step synthesis of symmetrical dialkyl trithiocarbonates

Yousefi, Ali

, p. 672 - 677 (2015/11/18)

Symmetrical dialkyl trithiocarbonates we...

822-38-8 Process route

1,4,6,9-tetrathiaspiro<4.4>nonane
13145-46-5

1,4,6,9-tetrathiaspiro<4.4>nonane

2-carboxybenzene diazonium chloride
4661-46-5

2-carboxybenzene diazonium chloride

1,3-dithiolane-2-thione
822-38-8

1,3-dithiolane-2-thione

2-thioxo-1,3-benzodithiole
934-36-1

2-thioxo-1,3-benzodithiole

phenylthioethylene
1822-73-7

phenylthioethylene

Conditions
Conditions Yield
With methyloxirane; In 1,2-dichloro-ethane; for 1h; Heating;
36%
15%
5%
carbon disulfide
75-15-0,12122-00-8

carbon disulfide

Li<sup>(1+)</sup>*OCD<sub>3</sub><sup>(1-)</sup>=LiOCD<sub>3</sub>

Li(1+)*OCD3(1-)=LiOCD3

thirane
420-12-2

thirane

1,3-dithiolane-2-thione
822-38-8

1,3-dithiolane-2-thione

Conditions
Conditions Yield
In d(4)-methanol; at 0 - 5 ℃; for 1h;
83%
17%

822-38-8 Upstream products

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    oxirane

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    carbon disulfide

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    1,3-dithiolane

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    1,2-ethanediyl bis(methyl trithiocarbonate)

822-38-8 Downstream products

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    3-Phenyl-1-oxa-4,6,9-trithiaspiro<4.4>nonan

  • 138197-05-4
    138197-05-4

    2-Phenyl-1,4,6,9-tetrathiaspiro<4.4>nonan

  • 82204-47-5
    82204-47-5

    Trithiocarbonic acid benzyl ester vinyl ester

  • 2314-61-6
    2314-61-6

    4-phenyl-1,3-dithiole-2-thione

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