197637
Imidazole sodium derivative
technical grade
Sinonimo/i:
Imidazolylsodium, Sodium imidazolide
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About This Item
Formula empirica (notazione di Hill):
C3H3N2Na
Numero CAS:
Peso molecolare:
90.06
Beilstein:
3569312
Numero CE:
Numero MDL:
Codice UNSPSC:
12352005
eCl@ss:
39161001
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Grado
technical grade
Punto di fusione
284 °C (dec.) (lit.)
Stringa SMILE
[Na]n1ccnc1
InChI
1S/C3H3N2.Na/c1-2-5-3-4-1;/h1-3H;/q-1;+1
ITAWMPSVROAMOE-UHFFFAOYSA-N
Applicazioni
Imidazole sodium derivative (Imidazolylsodium) was used in the synthesis of arylazidoamorphigenin.
Avvertenze
Danger
Indicazioni di pericolo
Classi di pericolo
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
Codice della classe di stoccaggio
8A - Combustible corrosive hazardous materials
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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F G Earley et al.
The Biochemical journal, 224(2), 525-534 (1984-12-01)
A photoaffinity-labelling analogue of the respiratory inhibitor rotenone was synthesized from the naturally occurring rotenoid amorphigenin. The analogue inhibits NADH-ubiquinone oxidoreductase activity at concentrations comparable with those of rotenone. Photolysis of the radiolabelled analogue bound to isolated NADH-ubiquinone oxidoreductase resulted
Richard C Knighton et al.
Chemical communications (Cambridge, England), 49(23), 2293-2295 (2013-02-15)
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Inorganic chemistry, 52(6), 3170-3177 (2013-03-09)
The effects of the deprotonation of coordinated imidazole on the vibrational dynamics of five-coordinate high-spin iron(II) porphyrinates have been investigated using nuclear resonance vibrational spectroscopy. Two complexes have been studied in detail with both powder and oriented single-crystal measurements. Changes
Ho Young Lee et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(14), 5416-5421 (2013-03-16)
RNA-binding proteins control the fate and function of the transcriptome in all cells. Here we present technology for isolating RNA-protein partners efficiently and accurately using an engineered clustered regularly interspaced short palindromic repeats (CRISPR) endoribonuclease. An inactive version of the
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