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About This Item
Linear Formula:
NaOCN
CAS Number:
Molecular Weight:
65.01
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
38060512
UNSPSC Code:
12161600
EC Number:
213-030-6
MDL number:
Beilstein/REAXYS Number:
3655041
InChI key
ZVCDLGYNFYZZOK-UHFFFAOYSA-M
InChI
1S/CHNO.Na/c2-1-3;/h3H;/q;+1/p-1
SMILES string
[Na+].[O-]C#N
assay
96%
reaction suitability
core: sodium, reagent type: catalyst
Quality Level
Related Categories
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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C Geers et al.
Comparative biochemistry and physiology. Part A, Physiology, 112(1), 111-117 (1995-09-01)
In isolated rat soleus and extensor digitorum longus (EDL) muscles, the effects of carbonic anhydrase inhibitors were studied on oxygen consumption as well as lactate release and accumulation after incubation in inhibitors lasting long enough to produce marked changes in
I Koshiishi et al.
Biochimica et biophysica acta, 1336(3), 566-574 (1997-11-21)
Ascorbate-dehydroascorbate redox cycle plays a key role in protecting organisms from an excess of oxidants. Recently, we found a novel reaction of dehydroascorbate with cyanate under the conditions of neutral pH and ordinary temperature. In this report, we demonstrated that
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Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology, 195(11), 1021-1030 (2009-09-26)
Ducks are well-known to be more tolerant to asphyxia than non-diving birds, but it is not known if their defences include enhanced neuronal hypoxia tolerance. To test this, we compared extracellular recordings of spontaneous activity in the Purkinje cell layer
Jay K Herman et al.
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The purpose of the present study was to use chemoafferent recordings from the goat carotid body (CB) to pharmacologically identify the putative low affinity excitatory receptor for dopamine (DA). Close arterial injections of DA (1-50 microg kg(-1)) induced a dose-dependent
Ekaterina V Vinogradova et al.
Organic letters, 15(6), 1394-1397 (2013-02-28)
An efficient synthesis of aryl carbamates was achieved by introducing alcohols into the reaction of palladium-catalyzed cross-coupling of ArX (X = Cl, OTf) with sodium cyanate. The use of aryl triflates as electrophilic components in this transformation allowed for an
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