197637
Imidazole sodium derivative
technical grade
Synonym(s):
Imidazolylsodium, Sodium imidazolide
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About This Item
Empirical Formula (Hill Notation):
C3H3N2Na
CAS Number:
Molecular Weight:
90.06
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39161001
UNSPSC Code:
12352005
EC Number:
226-988-5
MDL number:
Beilstein/REAXYS Number:
3569312
grade
technical grade
Quality Level
mp
284 °C (dec.) (lit.)
SMILES string
[Na]n1ccnc1
InChI
1S/C3H3N2.Na/c1-2-5-3-4-1;/h1-3H;/q-1;+1
InChI key
ITAWMPSVROAMOE-UHFFFAOYSA-N
Application
Imidazole sodium derivative (Imidazolylsodium) was used in the synthesis of arylazidoamorphigenin.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
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
Yun Dai et al.
Electrophoresis, 34(6), 833-840 (2013-01-22)
The first member of the single-isomer, dicationic cyclodextrin (CD) family, 6(A)-ammonium-6(C)-butylimidazolium-β-cyclodextrin chlorides (AMBIMCD), has been synthesized, analytically characterized, and used to separate a variety of acidic enantiomers and amino acids by CE. Starting from mono-6(A)-azido-β-cyclodextrin, the cationic imidazolium and ammonium
Kushal Sengupta et al.
Inorganic chemistry, 52(4), 2000-2014 (2013-01-30)
Electrodes bearing thiolate and imidazole coordinated iron porphyrin catalysts are constructed and characterized using resonance Raman spectroscopy, absorption spectroscopy, and electrochemistry. The cyclic voltammetry data and their pH dependences are used to establish the nature of the exchangeable trans ligands