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Merck

A7149

Sigma-Aldrich

Ammonium thiocyanate

powder

Sinónimos:

Ammonium rhodanide

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About This Item

Fórmula lineal:
NH4SCN
Número de CAS:
Peso molecular:
76.12
Beilstein/REAXYS Number:
3595135
EC Number:
MDL number:
UNSPSC Code:
12352300
eCl@ss:
38060604
PubChem Substance ID:
NACRES:
NA.55

vapor pressure

0.000114 hPa ( 20 °C)

assay

≥98% NaOH basis (titration)

form

powder

color

white

pH

4.8 (20.1 °C, 1070 g/L)

mp

152-154 °C (lit.)

solubility

water: soluble 76.1 g/L at 20 °C

SMILES string

N.SC#N

InChI

1S/CHNS.H3N/c2-1-3;/h3H;1H3

InChI key

SOIFLUNRINLCBN-UHFFFAOYSA-N

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General description

Ammonium thiocyanate is an ammonium salt commonly used for thiocyanation reaction of organic compounds.

Application

Ammonium thiocyanate (ATC) has been used for the preparation of epidermal sheets separated from the skin of the K14E7 mouse for immunofluorescence staining.
It may be used the synthesis of the following:
Ammonium thiocyanate (ATC) may be used the synthesis of the following:
  • Graphitic carbon nitride.
  • Three-dimensional nitrogen and sulfur co-doped graphene frameworks (N/S-GFs).
  • Substituted 2-aminothiazole derivatives by reacting with α-halo ketone carbonyls in the presence of N-methylimidazole.
  • Thiiranes from corresponding oxiranes in the presence of LiBF4.
  • 1,2,4-triazole-3-thiones by a multi-component reaction with benzohydrazide acid and acid chloride in the absence of solvent.

pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1

supp_hazards

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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Nor Malia Abd Warif et al.
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Thiocyanation of aromatic and heteroaromatic compounds using ammonium thiocyanate and I2O5.
Wu J, et al.
Synthetic Communications, 38(14), 2367-2373 (2008)
NBS or DEAD as effective reagents in α-thiocyanation of enolizable ketones with ammonium thiocyanate.
Reddy BVS, et al.
Tetrahedron Letters, 52(13), 1432-1435 (2011)
Regioselective thiocyanation of aromatic and heteroaromatic compounds using ammonium thiocyanate and oxone.
Wu G, et al.
Tetrahedron Letters, 46(35), 5831-5834 (2005)
Convenient and simple synthesis of 2-aminothiazoles by the reaction of α-halo ketone carbonyls with ammonium thiocyanate in the presence of N-methylimidazole.
Meshram HM, et al.
Tetrahedron Letters, 53(39), 5265-5269 (2012)

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