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Merck

161527

Sigma-Aldrich

Natriumhydrosulfid Hydrat

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About This Item

Lineare Formel:
NaSH·xH2O
CAS-Nummer:
Molekulargewicht:
56.06 (anhydrous basis)
MDL-Nummer:
UNSPSC-Code:
12352302
PubChem Substanz-ID:
NACRES:
NA.55

Form

chips
flakes

Konzentration

≥60% (by Na2S2O3, titration)

mp (Schmelzpunkt)

52-54 °C (lit.)

SMILES String

[Na]S.[H]O[H]

InChI

1S/Na.H2O.H2S/h;2*1H2/q+1;;/p-1

InChIKey

ZNKXTIAQRUWLRL-UHFFFAOYSA-M

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Allgemeine Beschreibung

Sodium hydrosulfide hydrate is a hydrated inorganic salt of sodium. It participates in the synthesis of (E)-2-cyano-2-(thiazolidin-2-ylidene)ethanethioamide.

Anwendung

It may be used as a sulfur nucleophile to induce the C-S bond formation in α,β-dichloro vinyl ketones to form 5- to 8-membered cyclic thioethers.
Sodium hydrosulfide hydrate may be used in the synthesis of following:
  • benzothiazole
  • 4-methoxybenzothioamide
  • 2-(4-methoxyphenyl)imidazoline
  • 7-chloro-4′-methoxythioflavone

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Oral - Aquatic Acute 1 - Skin Corr. 1B

Lagerklassenschlüssel

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

WGK

WGK 3

Flammpunkt (°F)

194.0 °F - closed cup

Flammpunkt (°C)

90 °C - closed cup


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Die Dokumentenbibliothek aufrufen

Mehdi Bakavoli et al.
Molecules (Basel, Switzerland), 14(12), 4849-4857 (2009-12-25)
Cyclocondensation of 2-[bis(methylthio)methylene]malononitrile (1) and cysteamine (2) afforded 2-(thiazolidin-2-ylidene)malononitrile (3). This compound on treatment with NaSH gave the corresponding thioamide derivative 4a in a regioselective manner on the basis of its single crystal X-ray diffraction analysis. Reaction of this compound
Bruna M Santos et al.
Acta physiologica (Oxford, England), 228(3), e13373-e13373 (2019-09-05)
Whereas some patients have important changes in body core temperature (Tb) during systemic inflammation, others maintain a normal Tb, which is intrinsically associated to immune paralysis. One classical model to study immune paralysis is the use of repeated administration of
Synthesis of Cyclic Thioethers through Tandem C(sp3)-S and C(sp2)-S Bond Formations from a, ? '-Dichloro Vinyl Ketones.
Oh K, et al.
The Journal of Organic Chemistry, 73(6), 2432-2434 (2008)
Honggang Wang et al.
Biology open, 8(7) (2019-07-19)
The aim of this study was to investigate whether exogenous hydrogen sulfide (H2S) could mitigate NLRP3 inflammasome-mediated inflammation through promoting autophagy via the AMPK-mTOR pathway in L02 cells. L02 cells were stimulated with different concentrations of oleic acid (OA), then
Synthesis of Benzothiazoles through Copper-Catalyzed One-Pot Three-Component Reactions with Use of Sodium Hydrosulfide as a Sulfur Surrogate.
Park N, et al.
European Journal of Organic Chemistry, 10, 1984-1993 (2012)

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