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
Beilstein:
3569312
EC Number:
MDL number:
UNSPSC Code:
12352005
eCl@ss:
39161001
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
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.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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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
Lizhen Qiao et al.
Journal of chromatography. A, 1286, 137-145 (2013-03-16)
Hydrophilic interaction liquid chromatography (HILIC) has been widely used for separating polar compounds as a complement mode to reversed-phase liquid chromatography. The development of new stationary phases for HILIC is significant to improve the coverage of various polar and hydrophilic
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
Yin Gao et al.
Bioorganic & medicinal chemistry, 21(5), 1305-1311 (2013-02-05)
Galactosyltransferases (GalTs) extend the glycan chains of mammalian glycoproteins by adding Gal to terminal GlcNAc residues, and thus build the scaffolds for biologically important glycan structures. We have shown that positively charged bivalent imidazolium salts in which the two imidazolium
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