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Thioacetamide information


Thioacetamide
Structural formula of thioacetamide
Ball-and-stick model of the thioacetamide molecule
Names
IUPAC name
Thioacetamide
Preferred IUPAC name
Ethanethioamide[1]
Other names
acetothioamide, TAA, thioacetimidic acid, TA, TAM
Identifiers
CAS Number
  • 62-55-5 checkY
3D model (JSmol)
  • Interactive image
Beilstein Reference
506006
ChEBI
  • CHEBI:32497 checkY
ChEMBL
  • ChEMBL38737 checkY
ChemSpider
  • 2006126 checkY
ECHA InfoCard 100.000.493 Edit this at Wikidata
EC Number
  • 200-541-4
KEGG
  • C19302 checkY
PubChem CID
  • 2723949
RTECS number
  • AC8925000
UNII
  • 075T165X8M checkY
UN number 3077
CompTox Dashboard (EPA)
  • DTXSID9021340 Edit this at Wikidata
InChI
  • InChI=1S/C2H5NS/c1-2(3)4/h1H3,(H2,3,4) checkY
    Key: YUKQRDCYNOVPGJ-UHFFFAOYSA-N checkY
  • InChI=1/C2H5NS/c1-2(3)4/h1H3,(H2,3,4)
    Key: YUKQRDCYNOVPGJ-UHFFFAOYAD
SMILES
  • S=C(N)C
Properties
Chemical formula
C2H5NS
Molar mass 75.13 g/mol
Appearance colourless crystals
Odor slight mercaptan
Density 1.319 g/cm3[2]
Melting point 115 °C (239 °F; 388 K)
Boiling point decomposes
Solubility in water
good
Magnetic susceptibility (χ)
-42.45·10−6 cm3/mol
Structure
Crystal structure
monoclinic
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Foul stench, carcinogenic
GHS labelling:
Pictograms
GHS07: Exclamation markGHS08: Health hazard
Signal word
Danger
Hazard statements
H302, H315, H319, H350, H412
Precautionary statements
P201, P202, P264, P270, P273, P280, P281, P301+P312, P302+P352, P305+P351+P338, P308+P313, P321, P330, P332+P313, P337+P313, P362, P405, P501
Safety data sheet (SDS) MSDS
Related compounds
Related compounds
acetamide, dithioacetic acid
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Thioacetamide is an organosulfur compound with the formula C2H5NS. This white crystalline solid is soluble in water and serves as a source of sulfide ions in the synthesis of organic and inorganic compounds. It is a prototypical thioamide.

  1. ^ International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. p. 856. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.
  2. ^ Cite error: The named reference Hurst was invoked but never defined (see the help page).

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Thioacetamide

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Thioacetamide is an organosulfur compound with the formula C2H5NS. This white crystalline solid is soluble in water and serves as a source of sulfide...

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Fibrosis

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formation of pseudolobules. Long-term exposure to hepatotoxins, such as thioacetamide, carbon tetrachloride, and diethylnitrosamine, has been shown to cause...

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Thioamide

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resulting in a larger rotational barrier. A well-known thioamide is thioacetamide, which is used as a source of the sulfide ion and is a building block...

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Centrilobular necrosis

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observation brought on by hepatotoxins like acetaminophen (paracetamol), thioacetamide, tetrachloride, cardiac hepatopathy due to acute right sided cardiac...

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Sirius Red

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Durgesh Kumar; Jena, G B (November 2018). "Glibenclamide protects against thioacetamide-induced hepatic damage in Wistar rat: investigation on NLRP3, MMP-2...

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Acetamide

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pharmaceuticals, pesticides, and antioxidants for plastics. It is a precursor to thioacetamide. Acetamide has been detected near the center of the Milky Way galaxy...

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IARC group 2B

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2-Tetrachloroethane Tetrachlorvinphos Tetrahydrofuran Tetranitromethane Thioacetamide 4,4'-Thiodianiline 2-Thiouracil Titanium dioxide Toluene diisocyanates...

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Hydrogen sulfide

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FeS + 2 HCl → FeCl2 + H2S For use in qualitative inorganic analysis, thioacetamide is used to generate H2S: CH3C(S)NH2 + H2O → CH3C(O)NH2 + H2S Many metal...

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Thiazole

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and thioamides. For example, 2,4-dimethylthiazole is synthesized from thioacetamide and chloroacetone. In the Cook-Heilbron synthesis, thiazoles arise by...

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California Proposition 65 list of chemicals

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Tetrafluoroethylene 116-14-3 Tetranitromethane 509-14-8 Thalidomide 50-35-1 Thioacetamide 62-55-5 Titanium dioxide 13463-67-7 4,4'-Thiodianiline 139-65-1 Thiodicarb...

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Avenciguat

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685509 Reduces Portal Hypertension and Portosystemic Shunting in a Rat Thioacetamide-Induced Cirrhosis Model". Journal of Pharmacology and Experimental Therapeutics...

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Tam

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tam, or -tam in Wiktionary, the free dictionary. TAM may refer to: Thioacetamide, an organosulfur compound Tumor-associated macrophage, a class of immune...

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Willgerodt rearrangement

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in a nucleophilic addition temporarily forming an aziridine and the thioacetamide by tautomerization. Willgerodt, Conrad (1887). "Ueber die Einwirkung...

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HL156A

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(October 2016). "AMP-activated protein kinase activator, HL156A reduces thioacetamide-induced liver fibrosis in mice and inhibits the activation of cultured...

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Jatrorrhizine

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antiinflammatory effect, and to improve blood flow and mitotic activity in thioacetamide-traumatized rat livers. It was found to have antimicrobial and antifungal...

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Qualitative inorganic analysis

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solutions; most commonly used are hydrogen sulfide (at 0.2-0.3 M), thioacetamide (at 0.3-0.6 M), addition of hydrogen sulfide can often prove to be a...

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Carleton Moore

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on The kinetics of the reactions of silver, lead, and thallium with thioacetamide, and The distribution of barium, titanium, manganese, chromium, iron...

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Ubiquitin B

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Goldknopf IL, Busch H (1981). "Protein A24 lyase activity in nucleoli of thioacetamide-treated rat liver releases histone 2A and ubiquitin from conjugated...

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Gustducin

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yet been established. PDE activation: Other bitter compounds, such as thioacetamide and propylthiouracil, have been shown[by whom?] to have stimulatory...

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List of compounds with carbon number 4

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38457-08-8 C4H9NO6 ammonium acid tartrate 3095-65-6 C4H9NS dimethyl thioacetamide 631-67-4 C4H9NS thiomorpholine 123-90-0 C4H9NSSi trimethylsilyl isothiocyanate...

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