4,5-Dichloro-1,2,3-dithiazolium chloride
- CAS No.
- 75318-43-3
- Chemical Name:
- 4,5-Dichloro-1,2,3-dithiazolium chloride
- Synonyms
- D14145;Appel salt;Appel's Salt;4,5-Dichlorodithiaz;4,5-dichlorodithiazol-1-ium;4,5-DICHLORO-1,2,3-DITHIAZOLIUM;4,5-Dichlorodithiazol-2-ium chloride;4,5-dichlorodithiazol-1-ium chloride;4,5-Dichloro-[1,2,3]dithiazol-2-ylium;4,5-Dichloro-1,2,3-dithiazolium chloride
- CBNumber:
- CB3511622
- Molecular Formula:
- C2Cl3NS2
- Molecular Weight:
- 208.5
- MDL Number:
- MFCD03426194
- MOL File:
- 75318-43-3.mol
| Melting point | 172° (dec) |
|---|---|
| storage temp. | under inert gas (nitrogen or Argon) at 2-8°C |
| form | solid |
| color | Brown |
| FDA UNII | 156NP9484D |
SAFETY
Risk and Safety Statements
| Symbol(GHS) |  GHS07 |
|---|---|
| Signal word | Warning |
| Hazard statements | H319-H335-H302+H312+H332-H315 |
| Precautionary statements | P280-P301+P312-P362+P364 |
| HS Code | 2934999090 |
4,5-Dichloro-1,2,3-dithiazolium chloride price More Price(21)
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| TRC | D432328 | 4,5-Dichloro-1,2,3-dithiazoliumchloride | 75318-43-3 | 500mg | $175 | 2021-12-16 | Buy |
| AK Scientific | 4308CS | 4,5-Dichloro-1,2,3-dithiazol-1-iumchloride | 75318-43-3 | 1g | $215 | 2021-12-16 | Buy |
| Biosynth Carbosynth | FD149446 | 4,5-Dichloro-1,2,3-dithiazoliumchloride | 75318-43-3 | 1g | $250 | 2021-12-16 | Buy |
| Biosynth Carbosynth | FD149446 | 4,5-Dichloro-1,2,3-dithiazoliumchloride | 75318-43-3 | 2g | $450 | 2021-12-16 | Buy |
| SynQuest Laboratories | 7H70-5-0LT | 4,5-Dichloro-1,2,3-dithiazol-2-yliumchloride tech% | 75318-43-3 | 5G | $453 | 2021-12-16 | Buy |
4,5-Dichloro-1,2,3-dithiazolium chloride Chemical Properties,Uses,Production
Description
4,5-Dichloro-1,2,3-dithiazolium chloride is an useful organosulfur compound. It is the chloride salt of the 4,5-dichloro-1,2,3-dithiazolium cation. It is a green solid that is poorly soluble in organic solvents. Most primary arylamines react readily with 4,5-dichloro-1,2,3-dithiazolium chloride to give, after treatment with tertiary amine base (2 equiv.), the corresponding N-aryl-4-chloro-5H-1,2,3-dithiazolimines in good to excellent yields. This compound is commonly used to synthesize monocyclic 1,2,3-dithiazoles which act as fungicides, antibacterials, antivirals or anticancer agents[1-2].
Uses
Synthon in heterocyclic chemistry; in conversion of alcohols and carboxylic acids to esters.
References
[1] Kalogirou A, et al. The Reaction of 4,5-Dichloro-1,2,3-dithiazolium Chloride with Sulfimides: A New Synthesis of N-Aryl-1,2,3-dithiazolimines. Molecules, 2009; 14: 2356–2362.
[2] Plakas K, et al. Reaction of 4,5-Dichloro-1,2,3-dithiazolium Chloride with 2-(Phenylsulfonyl)acetonitrile. Molbank, 2022; 2022: M1322.
4,5-Dichloro-1,2,3-dithiazolium chloride Preparation Products And Raw materials
4,5-Dichloro-1,2,3-dithiazolium chloride Suppliers
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
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